Article(id=1276175807659766492, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1276175380184695804, articleNumber=null, orderNo=null, doi=10.3969/j.issn.1000-2561.2024.09.001, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1676649600000, receivedDateStr=2023-02-18, revisedDate=1679241600000, revisedDateStr=2023-03-20, acceptedDate=null, acceptedDateStr=null, onlineDate=1782193622746, onlineDateStr=2026-06-23, pubDate=1727193600000, pubDateStr=2024-09-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782193622746, onlineIssueDateStr=2026-06-23, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782193622746, creator=13701087609, updateTime=1782193622746, updator=13701087609, issue=Issue{id=1276175380184695804, tenantId=1146029695717560320, journalId=1235980609244409860, year='2024', volume='45', issue='9', pageStart='1761', pageEnd='1997', issueExtLink='null', onlineDate='null', pubDate='1727193600000', pubDateStr='2024-09-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1782193520816, creator='13701087609', updateTime=1782193908264, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1276177005326504448, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1276175380184695804, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1276177005326504449, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1276175380184695804, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=1761, endPage=1779, ext={EN=ArticleExt(id=1276175809438151390, articleId=1276175807659766492, tenantId=1146029695717560320, journalId=1235980609244409860, language=EN, title=Genome-wide Identification and Expression Analysis of GRAS Gene Family in Hevea brasiliensis, columnId=1236256430337085821, journalTitle=Chinese Journal of Tropical Crops, columnName=Omics & Biotechnology, runingTitle=null, highlight=null, articleAbstract=

GRAS is a plant-specific transcription factor, which plays an important regulatory role in plant growth and development, and abiotic stress response. GRAS gene family has not been reported in Hevea brasiliensis. In this study, bioinformatics tools were used to analyze the physicochemical properties, phylogenetic relationships, gene structures, chromosome positions, and cis-acting elements of promoters of GRAS gene family members in H. brasiliensis. The expression patterns of HbGRAS were analyzed by transcriptome data and real-time quantitative PCR (qPCR). A total of 91 GRAS family members were identified from H. brasiliensis genome, named HbGRAS1HbGRAS91, with molecular weights ranging from 14.07–89.46 kDa. The results of subcellular localization prediction showed that HbGRAS was mainly localized in the nucleus and chloroplast. Those proteins were divided into 14 subfamilies based on phylogenetic analysis. The gene structures and motif compositions within the same subfamily were relatively conserved. The 91 GRAS family members were distributed in 17 chromosomes and two scaffolds except for chromosome 11 in rubber tree. We found that 17 HbGRAS genes were involved in 10 tandem repeat events. Collinearity analysis revealed the segmental duplication regions containing 87 HbGRAS genes, suggested that gene fragment duplication may be the major driver of GRAS gene expansion in H. brasiliensis. Cis-acting element prediction showed that HbGRAS family contained multiple phytohormone and stress-responsive elements. The expression patterns of HbGRAS genes had tissue specificity and were associated with leaf development. The expressions of DELLA genes, a member of the GRAS subfamily, were related to the xylem development and were repressed by gibberellin (GA). Those results provide a reference for functional research on the GRAS genes in rubber trees.

, authors=null, authorsList=Juan LI, Yuan YUAN, Tingkai WU, Zhi DENG, Han CHENG, authorCompany=null, correspAuthors=Zhi DENG, Han CHENG, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1276175823610704628, articleId=1276175807659766492, tenantId=1146029695717560320, journalId=1235980609244409860, language=CN, title=巴西橡胶树GRAS基因家族鉴定及表达分析, columnId=1236256430517440904, journalTitle=热带作物学报, columnName=组学与生物技术, runingTitle=null, highlight=null, articleAbstract=

GRAS是植物特有的转录因子,在植物生长发育过程以及非生物胁迫应答中具有重要的调控作用,然而在巴西橡胶树(Hevea brasiliensis)中还未见关于该基因家族的报道。本研究利用生物信息学工具分析巴西橡胶树GRAS基因家族成员的蛋白质理化性质、系统进化关系、基因结构、染色体位置及启动子顺式作用元件,利用转录组数据及实时荧光定量PCR(qPCR)分析橡胶树GRAS基因的表达模式。结果表明:在巴西橡胶树基因组中共鉴定到91个GRAS家族成员,分别命名为HbGRAS1~HbGRAS91,其分子量在14.07~89.46 kDa之间。亚细胞定位预测结果显示,HbGRAS蛋白主要定位于细胞核和叶绿体。系统发育分析将其划分为14个亚家族,同一亚族成员的基因结构和基序组成较为保守。橡胶树GRAS基因分布在除11号染色体外的其他17条染色体和2条Scaffold上,其中17个HbGRAS基因组成10个串联重复事件。共线性分析显示,片段重复区域中有87个HbGRAS基因,说明片段重复可能是橡胶树GRAS基因扩张的主要驱动力。启动子顺式作用元件分析显示,橡胶树GRAS家族包含多个植物激素和胁迫应答顺式作用元件。HbGRAS基因表达具有组织特异性,并与橡胶树叶片发育有关。GRAS亚家族成员DELLA基因的表达与橡胶树木质部发育有关并受赤霉素(gibberellin,GA)抑制。本研究结果为橡胶树GRAS基因的功能研究提供参考。

, authors=

李娟(1998—),女,硕士研究生,研究方向:作物遗传资源研究与利用。

, authorsList=李娟, 袁渊, 吴挺开, 邓治, 程汉, authorCompany=null, correspAuthors=邓治, 程汉, authorNote=null, correspAuthorsNote=
* 邓治(DENG Zhi),E-mail:
程汉(CHENG Han),E-mail:
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2.Rubber Research Institute, Chinese Academy of Tropical Agricultural Science / National Key Laboratory of Tropical Crop Breeding, Haikou, Hainan 571101, China
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李娟(1998—),女,硕士研究生,研究方向:作物遗传资源研究与利用。

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李娟(1998—),女,硕士研究生,研究方向:作物遗传资源研究与利用。

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A: Phylogenetic tree; B: GRAS protein motif distribution; C: GRAS protein domain location; D: GRAS gene structure.

, figureFileSmall=nMwgntV+x+eV/9og8llgaA==, figureFileBig=XzWeYT/xy56IdxV54d09Pw==, tableContent=null), ArticleFig(id=1276465481821319836, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图2, caption=橡胶树GRAS蛋白序列的结构特征

A:系统进化树;B:GRAS蛋白基序分布;C:GRAS蛋白结构域位置;D:GRAS基因结构。

, figureFileSmall=nMwgntV+x+eV/9og8llgaA==, figureFileBig=XzWeYT/xy56IdxV54d09Pw==, tableContent=null), ArticleFig(id=1276465481905205917, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 3, caption=Chromosomal localization of GRAS genes in H. brasiliensis

Red font indicates the tandem duplication genes, red line indicates a series of tandem repetition events.

, figureFileSmall=4u22V4G9o+Og0gjOnbDH/Q==, figureFileBig=miR+yj9pPlUNUNOvgWcYzQ==, tableContent=null), ArticleFig(id=1276465481984897694, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图3, caption=橡胶树GRAS基因的染色体定位

红色字体表示串联重复基因,红色线条表示串联重复事件。

, figureFileSmall=4u22V4G9o+Og0gjOnbDH/Q==, figureFileBig=miR+yj9pPlUNUNOvgWcYzQ==, tableContent=null), ArticleFig(id=1276465482060395167, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 4, caption=Collinearity analysis of GRAS genes in H. brasiliensis, figureFileSmall=FKjhB5zoLxFtq82g+e6cGQ==, figureFileBig=bKKMAIeFIS9dw8IJAOMs3A==, tableContent=null), ArticleFig(id=1276465482127504032, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图4, caption=橡胶树GRAS基因的共线性分析, figureFileSmall=FKjhB5zoLxFtq82g+e6cGQ==, figureFileBig=bKKMAIeFIS9dw8IJAOMs3A==, tableContent=null), ArticleFig(id=1276465482257527457, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 5, caption=Prediction of cis-acting element in the promoter region of rubber tree GRAS genes, figureFileSmall=OgRgHw7/tag3Vb9uSG8diA==, figureFileBig=zxEEJXSk4F5kXuSuROD5KQ==, tableContent=null), ArticleFig(id=1276465482349802146, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图5, caption=橡胶树GRAS基因启动子区域的顺式作用元件预测, figureFileSmall=OgRgHw7/tag3Vb9uSG8diA==, figureFileBig=zxEEJXSk4F5kXuSuROD5KQ==, tableContent=null), ArticleFig(id=1276465482416911011, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 6, caption=Expression patterns of HbGRAS genes in different tissues of H. brasiliensis, figureFileSmall=pPwnka6ZVtU/uPZLSSt45Q==, figureFileBig=6jlNEm/MwJD/LBiRNe6Wbw==, tableContent=null), ArticleFig(id=1276465482479825572, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图6, caption=橡胶树不同组织中HbGRAS基因表达模式, figureFileSmall=pPwnka6ZVtU/uPZLSSt45Q==, figureFileBig=6jlNEm/MwJD/LBiRNe6Wbw==, tableContent=null), ArticleFig(id=1276465482538545829, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 7, caption=Expression patterns of HbGRAS genes in leaves at different developmental stages of H. brasiliensis, figureFileSmall=vGRU/Xcv6ZhWbYuByNxuuA==, figureFileBig=x8KQ4f4FKg/IS11iPXCl4A==, tableContent=null), ArticleFig(id=1276465482601460390, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图7, caption=橡胶树不同叶片发育时期中HbGRAS基因表达模式, figureFileSmall=vGRU/Xcv6ZhWbYuByNxuuA==, figureFileBig=x8KQ4f4FKg/IS11iPXCl4A==, tableContent=null), ArticleFig(id=1276465482668569255, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 8, caption=Expression patterns of HbDELLA genes in different tissues of H. brasiliensis

Different lowercase letters indicate significant difference (P<0.05).

, figureFileSmall=h1mA64BFlPLlwX3jfCLv0g==, figureFileBig=SjCQFXCLSrvB8+RKa/wubA==, tableContent=null), ArticleFig(id=1276465482756649640, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图8, caption=橡胶树不同组织中HbDELLA基因表达模式

不同小写字母表示差异显著(P<0.05)。

, figureFileSmall=h1mA64BFlPLlwX3jfCLv0g==, figureFileBig=SjCQFXCLSrvB8+RKa/wubA==, tableContent=null), ArticleFig(id=1276465482832147113, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 9, caption=Expression patterns of HbDELLA genes in different internodes of H. brasiliensis

Different lowercase letters indicate significant difference (P<0.05).

, figureFileSmall=cJNsjYDOlTP0LyIjlD/oJg==, figureFileBig=LpyzdMsOLh1Tvgq2fWDd8w==, tableContent=null), ArticleFig(id=1276465482903450282, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图9, caption=橡胶树不同节间中HbDELLA基因表达模式

不同小写字母表示差异显著(P<0.05)。

, figureFileSmall=cJNsjYDOlTP0LyIjlD/oJg==, figureFileBig=LpyzdMsOLh1Tvgq2fWDd8w==, tableContent=null), ArticleFig(id=1276465482987336363, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Fig. 10, caption=Expression patterns of HbDELLA genes under GA3 treatment of H. brasiliensis

Different lowercase letters indicate significant difference (P<0.05).

, figureFileSmall=wiwscpiwkh0/Y5ponZ0JQA==, figureFileBig=o4QMcxVAXHytNhOHRnuUew==, tableContent=null), ArticleFig(id=1276465483058639532, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=图10, caption=GA3处理下橡胶树HbDELLA基因表达模式

不同小写字母表示差异显著(P<0.05)。

, figureFileSmall=wiwscpiwkh0/Y5ponZ0JQA==, figureFileBig=o4QMcxVAXHytNhOHRnuUew==, tableContent=null), ArticleFig(id=1276465483121554093, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Tab. 1, caption=

Primers for qPCR

, figureFileSmall=null, figureFileBig=null, tableContent=
引物名称Primer name正向引物(5ʹ-3ʹ)Forward primer(5ʹ-3ʹ)反向引物(5ʹ-3ʹ)Reverse primer(5ʹ-3ʹ)
YLS8CCTCGTCGTCATCCGATTCCAGGCACCTCAGTGATGTC
HbGRAS44TGGGCCTGATTCTGGTAACACAACCGTAATTGTTGACGCAGG
HbGRAS58TTAACTGGCATTGGCCCTCCCCACGGAAAGCGAATCGAAC
HbGRAS62CCTACATCGCCTTCAACCACCAAAGGAGCCACCAACCGTA
HbGRAS64AGCACAGTCGAGATGTGGTGGGTCTGTGGTTGCGGATTTC
HbGRAS82GCCGCCTCTCTTAGCTGATGAGTGTGTGTACGAGACGGAC
HbGRAS89ACGAAGGAGAGATCCAAATCGCAAGAAGCATCAGTATTGGTA
), ArticleFig(id=1276465483188662958, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=表1, caption=

qPCR引物

, figureFileSmall=null, figureFileBig=null, tableContent=
引物名称Primer name正向引物(5ʹ-3ʹ)Forward primer(5ʹ-3ʹ)反向引物(5ʹ-3ʹ)Reverse primer(5ʹ-3ʹ)
YLS8CCTCGTCGTCATCCGATTCCAGGCACCTCAGTGATGTC
HbGRAS44TGGGCCTGATTCTGGTAACACAACCGTAATTGTTGACGCAGG
HbGRAS58TTAACTGGCATTGGCCCTCCCCACGGAAAGCGAATCGAAC
HbGRAS62CCTACATCGCCTTCAACCACCAAAGGAGCCACCAACCGTA
HbGRAS64AGCACAGTCGAGATGTGGTGGGTCTGTGGTTGCGGATTTC
HbGRAS82GCCGCCTCTCTTAGCTGATGAGTGTGTGTACGAGACGGAC
HbGRAS89ACGAAGGAGAGATCCAAATCGCAAGAAGCATCAGTATTGGTA
), ArticleFig(id=1276465483259966127, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Tab. 2, caption=

Physicochemical properties and subcellular localization prediction of GRAS gene family in Hevea brasiliensis

, figureFileSmall=null, figureFileBig=null, tableContent=
基因名称Gene name基因ID Gene ID氨基酸长度Length of amino acid分子量Molecular weight/kDa等电点Isoelectric point总平均疏水性Total mean hydrophobicity亚细胞定位预测Subcellular location prediction
HbGRAS1HB1G00388.t142347.705.21–0.418细胞核
HbGRAS2HB1G01849.t155562.095.66–0.628细胞核
HbGRAS3HB1G02033.t147853.925.87–0.153叶绿体
HbGRAS4HB2G00960.t144649.586.34–0.117细胞核
HbGRAS5HB2G01656.t159668.046.69–0.343叶绿体
HbGRAS6HB2G02237.t172179.035.24–0.273细胞核
HbGRAS7HB3G01006.t155362.165.64–0.311细胞核
HbGRAS8HB3G01280.t152559.514.80–0.334叶绿体
HbGRAS9HB3G01371.t182489.466.09–0.298细胞核
HbGRAS10HB4G00114.t138142.225.19–0.084叶绿体
HbGRAS11HB4G00115.t149755.836.02–0.245叶绿体
HbGRAS12HB4G00116.t132636.577.610.073质膜
HbGRAS13HB4G00119.t157064.845.01–0.268叶绿体
HbGRAS14HB4G00120.t141646.838.25–0.018叶绿体
HbGRAS15HB4G00841.t153559.084.89–0.195细胞核
HbGRAS16HB4G01021.t156963.285.88–0.393细胞核
HbGRAS17HB5G00086.t178485.185.82–0.328细胞核
HbGRAS18HB5G00100.t178485.195.90–0.334细胞核
HbGRAS19HB5G00848.t151959.144.93–0.403叶绿体
HbGRAS20HB5G01030.t174785.456.45–0.593叶绿体
HbGRAS21HB5G01034.t157365.859.07–0.558叶绿体
HbGRAS22HB5G01163.t154361.025.39–0.314细胞核
HbGRAS23HB5G01220.t144147.815.77–0.181叶绿体
HbGRAS24HB6G00656.t145751.505.27–0.431细胞核
HbGRAS25HB6G01072.t166473.376.06–0.341细胞核
HbGRAS26HB6G01076.t168375.375.82–0.355细胞核
HbGRAS27HB6G01628.t154260.825.93–0.656细胞核
HbGRAS28HB6G01802.t147553.495.92–0.166叶绿体
HbGRAS29HB7G00201.t150055.905.96–0.172细胞核
HbGRAS30HB7G00392.t151957.716.05–0.149细胞核
HbGRAS31HB7G00738.t154260.515.63–0.242细胞核
HbGRAS32HB7G01350.t140145.065.290.082质膜
HbGRAS33HB7G01368.t150156.695.43–0.419叶绿体
HbGRAS34HB7G01749.t148856.235.03–0.149叶绿体
HbGRAS35HB8G01417.t175184.076.04–0.396叶绿体
HbGRAS36HB9G00100.t172679.325.91–0.241细胞核
HbGRAS37HB9G01011.t145050.715.82–0.088叶绿体
HbGRAS38HB9G01128.t176585.975.54–0.513细胞核
HbGRAS39HB9G01129.t179188.675.26–0.533细胞核
HbGRAS40HB9G01130.t159367.645.88–0.279叶绿体
HbGRAS41HB9G01131.t169579.106.16–0.613细胞核
HbGRAS42HB9G01132.t168277.605.99–0.556细胞核
HbGRAS43HB9G01532.t160666.294.97–0.282细胞核
HbGRAS44HB9G01717.t161666.935.24–0.269细胞核
HbGRAS45HB9G02123.t178886.336.52–0.348细胞核
HbGRAS46HB9G02263.t166574.135.72–0.384细胞核
HbGRAS47HB9G02672.t144849.736.05–0.094细胞核
HbGRAS48HB10G00207.t150956.996.30–0.187细胞核
HbGRAS49HB10G00413.t148154.055.53–0.128质膜
HbGRAS50HB10G00730.t154161.315.75–0.308细胞核
HbGRAS51HB10G00901.t144549.795.42–0.174叶绿体
HbGRAS52HB10G01429.t150056.615.39–0.383叶绿体
HbGRAS53HB10G01450.t146151.605.59–0.060叶绿体
HbGRAS54HB10G01677.t151557.785.99–0.070细胞质
HbGRAS55HB12G00727.t148653.705.55–0.253叶绿体
HbGRAS56HB12G00826.t158665.584.94–0.370细胞核
HbGRAS57HB12G01212.t146052.286.35–0.363叶绿体
HbGRAS58HB13G00766.t153858.905.43–0.065细胞核
HbGRAS59HB13G01444.t142747.645.500.020叶绿体
HbGRAS60HB13G01796.t163569.426.24–0.400细胞核
HbGRAS61HB13G02058.t149043.754.880.151细胞质
HbGRAS62HB14G00396.t144148.475.29–0.097叶绿体
HbGRAS63HB14G01685.t174883.525.84–0.397叶绿体
HbGRAS64HB15G00806.t163469.905.50–0.297细胞核
HbGRAS65HB15G01391.t156963.255.79–0.389细胞核
HbGRAS66HB15G01391.t1.1.5e73594854160.285.71–0.419细胞核
HbGRAS67HB15G01545.t152958.685.22–0.276细胞核
HbGRAS68HB15G02227.t158666.205.01–0.166叶绿体
HbGRAS69HB16G00119.t144650.255.10–0.077叶绿体
HbGRAS70HB16G00306.t159967.344.72–0.111叶绿体
HbGRAS71HB16G00448.t145752.196.18–0.328叶绿体
HbGRAS72HB16G00620.t158665.945.05–0.395细胞核
HbGRAS73HB16G00747.t149454.535.69–0.214叶绿体
HbGRAS74HB16G00950.t145050.706.06–0.107叶绿体
HbGRAS75HB16G01057.t179989.215.22–0.454细胞核
HbGRAS76HB16G01058.t175784.965.35–0.483细胞核
HbGRAS77HB16G01059.t160067.786.23–0.251叶绿体
HbGRAS78HB16G01060.t170179.845.59–0.564过氧化物酶体
HbGRAS79HB16G01061.t168978.375.79–0.594细胞核
HbGRAS80HB16G01062.t168277.495.69–0.427叶绿体
HbGRAS81HB16G01451.t160766.885.14–0.300细胞核
HbGRAS82HB16G01623.t161366.455.19–0.229细胞核
HbGRAS83HB16G01816.t141746.747.29–0.101叶绿体
HbGRAS84HB16G02038.t178085.456.12–0.309细胞核
HbGRAS85HB16G02170.t166673.995.94–0.407细胞核
HbGRAS86HB17G00055.t152958.964.85–0.246细胞核
HbGRAS87HB17G00303.t163569.427.56–0.404细胞核
HbGRAS88HB17G00644.t152158.055.66–0.093叶绿体
HbGRAS89HB18G00909.t163269.385.40–0.256细胞核
HbGRAS90Scaf402_G00001.t141246.585.11–0.459细胞核
HbGRAS91Scaf409_G00006.t111714.075.49–0.642叶绿体
), ArticleFig(id=1276465483339657904, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=CN, label=表2, caption=

橡胶树GRAS基因家族理化性质及亚细胞定位预测

, figureFileSmall=null, figureFileBig=null, tableContent=
基因名称Gene name基因ID Gene ID氨基酸长度Length of amino acid分子量Molecular weight/kDa等电点Isoelectric point总平均疏水性Total mean hydrophobicity亚细胞定位预测Subcellular location prediction
HbGRAS1HB1G00388.t142347.705.21–0.418细胞核
HbGRAS2HB1G01849.t155562.095.66–0.628细胞核
HbGRAS3HB1G02033.t147853.925.87–0.153叶绿体
HbGRAS4HB2G00960.t144649.586.34–0.117细胞核
HbGRAS5HB2G01656.t159668.046.69–0.343叶绿体
HbGRAS6HB2G02237.t172179.035.24–0.273细胞核
HbGRAS7HB3G01006.t155362.165.64–0.311细胞核
HbGRAS8HB3G01280.t152559.514.80–0.334叶绿体
HbGRAS9HB3G01371.t182489.466.09–0.298细胞核
HbGRAS10HB4G00114.t138142.225.19–0.084叶绿体
HbGRAS11HB4G00115.t149755.836.02–0.245叶绿体
HbGRAS12HB4G00116.t132636.577.610.073质膜
HbGRAS13HB4G00119.t157064.845.01–0.268叶绿体
HbGRAS14HB4G00120.t141646.838.25–0.018叶绿体
HbGRAS15HB4G00841.t153559.084.89–0.195细胞核
HbGRAS16HB4G01021.t156963.285.88–0.393细胞核
HbGRAS17HB5G00086.t178485.185.82–0.328细胞核
HbGRAS18HB5G00100.t178485.195.90–0.334细胞核
HbGRAS19HB5G00848.t151959.144.93–0.403叶绿体
HbGRAS20HB5G01030.t174785.456.45–0.593叶绿体
HbGRAS21HB5G01034.t157365.859.07–0.558叶绿体
HbGRAS22HB5G01163.t154361.025.39–0.314细胞核
HbGRAS23HB5G01220.t144147.815.77–0.181叶绿体
HbGRAS24HB6G00656.t145751.505.27–0.431细胞核
HbGRAS25HB6G01072.t166473.376.06–0.341细胞核
HbGRAS26HB6G01076.t168375.375.82–0.355细胞核
HbGRAS27HB6G01628.t154260.825.93–0.656细胞核
HbGRAS28HB6G01802.t147553.495.92–0.166叶绿体
HbGRAS29HB7G00201.t150055.905.96–0.172细胞核
HbGRAS30HB7G00392.t151957.716.05–0.149细胞核
HbGRAS31HB7G00738.t154260.515.63–0.242细胞核
HbGRAS32HB7G01350.t140145.065.290.082质膜
HbGRAS33HB7G01368.t150156.695.43–0.419叶绿体
HbGRAS34HB7G01749.t148856.235.03–0.149叶绿体
HbGRAS35HB8G01417.t175184.076.04–0.396叶绿体
HbGRAS36HB9G00100.t172679.325.91–0.241细胞核
HbGRAS37HB9G01011.t145050.715.82–0.088叶绿体
HbGRAS38HB9G01128.t176585.975.54–0.513细胞核
HbGRAS39HB9G01129.t179188.675.26–0.533细胞核
HbGRAS40HB9G01130.t159367.645.88–0.279叶绿体
HbGRAS41HB9G01131.t169579.106.16–0.613细胞核
HbGRAS42HB9G01132.t168277.605.99–0.556细胞核
HbGRAS43HB9G01532.t160666.294.97–0.282细胞核
HbGRAS44HB9G01717.t161666.935.24–0.269细胞核
HbGRAS45HB9G02123.t178886.336.52–0.348细胞核
HbGRAS46HB9G02263.t166574.135.72–0.384细胞核
HbGRAS47HB9G02672.t144849.736.05–0.094细胞核
HbGRAS48HB10G00207.t150956.996.30–0.187细胞核
HbGRAS49HB10G00413.t148154.055.53–0.128质膜
HbGRAS50HB10G00730.t154161.315.75–0.308细胞核
HbGRAS51HB10G00901.t144549.795.42–0.174叶绿体
HbGRAS52HB10G01429.t150056.615.39–0.383叶绿体
HbGRAS53HB10G01450.t146151.605.59–0.060叶绿体
HbGRAS54HB10G01677.t151557.785.99–0.070细胞质
HbGRAS55HB12G00727.t148653.705.55–0.253叶绿体
HbGRAS56HB12G00826.t158665.584.94–0.370细胞核
HbGRAS57HB12G01212.t146052.286.35–0.363叶绿体
HbGRAS58HB13G00766.t153858.905.43–0.065细胞核
HbGRAS59HB13G01444.t142747.645.500.020叶绿体
HbGRAS60HB13G01796.t163569.426.24–0.400细胞核
HbGRAS61HB13G02058.t149043.754.880.151细胞质
HbGRAS62HB14G00396.t144148.475.29–0.097叶绿体
HbGRAS63HB14G01685.t174883.525.84–0.397叶绿体
HbGRAS64HB15G00806.t163469.905.50–0.297细胞核
HbGRAS65HB15G01391.t156963.255.79–0.389细胞核
HbGRAS66HB15G01391.t1.1.5e73594854160.285.71–0.419细胞核
HbGRAS67HB15G01545.t152958.685.22–0.276细胞核
HbGRAS68HB15G02227.t158666.205.01–0.166叶绿体
HbGRAS69HB16G00119.t144650.255.10–0.077叶绿体
HbGRAS70HB16G00306.t159967.344.72–0.111叶绿体
HbGRAS71HB16G00448.t145752.196.18–0.328叶绿体
HbGRAS72HB16G00620.t158665.945.05–0.395细胞核
HbGRAS73HB16G00747.t149454.535.69–0.214叶绿体
HbGRAS74HB16G00950.t145050.706.06–0.107叶绿体
HbGRAS75HB16G01057.t179989.215.22–0.454细胞核
HbGRAS76HB16G01058.t175784.965.35–0.483细胞核
HbGRAS77HB16G01059.t160067.786.23–0.251叶绿体
HbGRAS78HB16G01060.t170179.845.59–0.564过氧化物酶体
HbGRAS79HB16G01061.t168978.375.79–0.594细胞核
HbGRAS80HB16G01062.t168277.495.69–0.427叶绿体
HbGRAS81HB16G01451.t160766.885.14–0.300细胞核
HbGRAS82HB16G01623.t161366.455.19–0.229细胞核
HbGRAS83HB16G01816.t141746.747.29–0.101叶绿体
HbGRAS84HB16G02038.t178085.456.12–0.309细胞核
HbGRAS85HB16G02170.t166673.995.94–0.407细胞核
HbGRAS86HB17G00055.t152958.964.85–0.246细胞核
HbGRAS87HB17G00303.t163569.427.56–0.404细胞核
HbGRAS88HB17G00644.t152158.055.66–0.093叶绿体
HbGRAS89HB18G00909.t163269.385.40–0.256细胞核
HbGRAS90Scaf402_G00001.t141246.585.11–0.459细胞核
HbGRAS91Scaf409_G00006.t111714.075.49–0.642叶绿体
), ArticleFig(id=1276465483478069937, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276175807659766492, language=EN, label=Tab. 3, caption=

Numbers of GRAS subfamilies among different plants

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亚家族名称Subfamily name橡胶树H. brasiliensis拟南芥A. thaliana水稻O. sativa毛果杨P. trichocarpa
LISCL1671012
PAT1136711
HAM115714
SHR103510
Os48014
Pt208008
DELLA65314
SCR6257
SCL35174
SCL4/72212
DLT2112
LAS2123
Os192012
Os432011
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不同植物间GRAS各亚家族数量

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亚家族名称Subfamily name橡胶树H. brasiliensis拟南芥A. thaliana水稻O. sativa毛果杨P. trichocarpa
LISCL1671012
PAT1136711
HAM115714
SHR103510
Os48014
Pt208008
DELLA65314
SCR6257
SCL35174
SCL4/72212
DLT2112
LAS2123
Os192012
Os432011
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巴西橡胶树GRAS基因家族鉴定及表达分析
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李娟 1, 2, 3 , 袁渊 2, 3 , 吴挺开 2, 3 , 邓治 2, 3, * , 程汉 2, 3, *
热带作物学报 | 组学与生物技术 2024,45(9): 1761-1779
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热带作物学报 |组学与生物技术 2024 , 45 (9) : 1761 -1779
巴西橡胶树GRAS基因家族鉴定及表达分析
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李娟1, 2, 3, 袁渊2, 3, 吴挺开2, 3, 邓治2, 3, * , 程汉2, 3, *
作者信息
  • 1.浙江农林大学现代农学院,浙江杭州 311300
  • 2.中国热带农业科学院橡胶研究所/热带作物生物育种全国重点实验室,海南海口 571101
  • 3.中国热带农业科学院三亚研究院,海南三亚 572025
通讯作者:
* 邓治(DENG Zhi),E-mail:
程汉(CHENG Han),E-mail:
Genome-wide Identification and Expression Analysis of GRAS Gene Family in Hevea brasiliensis
Juan LI1, 2, 3, Yuan YUAN2, 3, Tingkai WU2, 3, Zhi DENG2, 3, * , Han CHENG2, 3, *
Affiliations
  • 1.College of Advanced Agricultural Sciences, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China
  • 2.Rubber Research Institute, Chinese Academy of Tropical Agricultural Science / National Key Laboratory of Tropical Crop Breeding, Haikou, Hainan 571101, China
  • 3.Sanya Research Institute, Chinese Academy of Tropical Agricultural Sciences, Sanya, Hainan 572025, China
出版时间: 2024-09-25 doi: 10.3969/j.issn.1000-2561.2024.09.001
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GRAS是植物特有的转录因子,在植物生长发育过程以及非生物胁迫应答中具有重要的调控作用,然而在巴西橡胶树(Hevea brasiliensis)中还未见关于该基因家族的报道。本研究利用生物信息学工具分析巴西橡胶树GRAS基因家族成员的蛋白质理化性质、系统进化关系、基因结构、染色体位置及启动子顺式作用元件,利用转录组数据及实时荧光定量PCR(qPCR)分析橡胶树GRAS基因的表达模式。结果表明:在巴西橡胶树基因组中共鉴定到91个GRAS家族成员,分别命名为HbGRAS1~HbGRAS91,其分子量在14.07~89.46 kDa之间。亚细胞定位预测结果显示,HbGRAS蛋白主要定位于细胞核和叶绿体。系统发育分析将其划分为14个亚家族,同一亚族成员的基因结构和基序组成较为保守。橡胶树GRAS基因分布在除11号染色体外的其他17条染色体和2条Scaffold上,其中17个HbGRAS基因组成10个串联重复事件。共线性分析显示,片段重复区域中有87个HbGRAS基因,说明片段重复可能是橡胶树GRAS基因扩张的主要驱动力。启动子顺式作用元件分析显示,橡胶树GRAS家族包含多个植物激素和胁迫应答顺式作用元件。HbGRAS基因表达具有组织特异性,并与橡胶树叶片发育有关。GRAS亚家族成员DELLA基因的表达与橡胶树木质部发育有关并受赤霉素(gibberellin,GA)抑制。本研究结果为橡胶树GRAS基因的功能研究提供参考。

巴西橡胶树  /  GRAS基因家族  /  生物信息学  /  基因表达  /  DELLA

GRAS is a plant-specific transcription factor, which plays an important regulatory role in plant growth and development, and abiotic stress response. GRAS gene family has not been reported in Hevea brasiliensis. In this study, bioinformatics tools were used to analyze the physicochemical properties, phylogenetic relationships, gene structures, chromosome positions, and cis-acting elements of promoters of GRAS gene family members in H. brasiliensis. The expression patterns of HbGRAS were analyzed by transcriptome data and real-time quantitative PCR (qPCR). A total of 91 GRAS family members were identified from H. brasiliensis genome, named HbGRAS1HbGRAS91, with molecular weights ranging from 14.07–89.46 kDa. The results of subcellular localization prediction showed that HbGRAS was mainly localized in the nucleus and chloroplast. Those proteins were divided into 14 subfamilies based on phylogenetic analysis. The gene structures and motif compositions within the same subfamily were relatively conserved. The 91 GRAS family members were distributed in 17 chromosomes and two scaffolds except for chromosome 11 in rubber tree. We found that 17 HbGRAS genes were involved in 10 tandem repeat events. Collinearity analysis revealed the segmental duplication regions containing 87 HbGRAS genes, suggested that gene fragment duplication may be the major driver of GRAS gene expansion in H. brasiliensis. Cis-acting element prediction showed that HbGRAS family contained multiple phytohormone and stress-responsive elements. The expression patterns of HbGRAS genes had tissue specificity and were associated with leaf development. The expressions of DELLA genes, a member of the GRAS subfamily, were related to the xylem development and were repressed by gibberellin (GA). Those results provide a reference for functional research on the GRAS genes in rubber trees.

Hevea brasiliensis  /  GRAS gene family  /  bioinformatics analysis  /  gene expression  /  DELLA
李娟, 袁渊, 吴挺开, 邓治, 程汉. 巴西橡胶树GRAS基因家族鉴定及表达分析. 热带作物学报, 2024 , 45 (9) : 1761 -1779 . DOI: 10.3969/j.issn.1000-2561.2024.09.001
Juan LI, Yuan YUAN, Tingkai WU, Zhi DENG, Han CHENG. Genome-wide Identification and Expression Analysis of GRAS Gene Family in Hevea brasiliensis[J]. Chinese Journal of Tropical Crops, 2024 , 45 (9) : 1761 -1779 . DOI: 10.3969/j.issn.1000-2561.2024.09.001
转录因子(transcription factor,TF)是功能基因组学的核心,它是一种能与特异DNA序列结合的蛋白,可以单独或与其他蛋白形成复合体,提高或阻断特定基因RNA聚合酶的招募,调控基因的表达[1]。转录因子在调控高等植物的生长发育和非生物胁迫响应中起重要作用[2]。已知的转录因子包括GRAS、WRKY、AP2/EREBP、bZIP、MYB、MADS和bHLH等。
GRAS家族是一类植物特有的转录因子,其命名来源于该家族最早鉴定的3个功能特征基因GAI(gibberellic-acid insensitive)、RGA(repressor of GA1-3 mutant)、SCR(scarecrow)[3-5]。GRAS蛋白的长度为400~770个氨基酸不等,具有1个高度保守的C-端GRAS结构域。GRAS结构域约390个氨基酸,由5个不同基序按照特定顺序排列组成:LHR I(leucine heptad repeat I)、VHIID、LHR II(leucine heptad repeat II)、PFYRE和SAW[6]。其中,VHIID基序与2个亮氨酸七肽重复区(LHR I和LHR II)结合形成LHR I-VHIID-LHR II复合体,该结构可能在蛋白-DNA或蛋白-蛋白互作中发挥关键功能[7]。PFYRE和SAW基序功能仍未阐明,但这2个基序发生缺失或错义突变导致拟南芥(Arabidopsis thaliana)表型异常[4,8]。GRAS蛋白的N端保守性较差,但一些GRAS家族成员在N端区域含有保守的序列,如DELLA亚家族包含2个保守的基序DELLA和TVHYNP[9]。最初根据拟南芥和水稻的研究将GRAS家族分为DELLA、HAM(hairy meristem)、PAT1(phytochrome a signal transduction 1)、LAS(lateral suppressor)、SHR(short root)、SCR、SCL3(SCR- like 3)、LISCL(lilium longiflorum SCR-like)等8个亚家族。而其他植物物种,如番茄(Solanum lycopersicum[10]、茶树(Camellia sinensis[11]和葡萄(Vitis vinifera[12]中有13个亚家族,葫芦(Lagenaria siceraria[13]中有16个亚家族,CENCI等[14]将被子植物GRAS家族分为17个亚家族。目前,GRAS基因家族已在多个物种中被报道,其中拟南芥(Arabidopsis thaliana[15]有33个成员、水稻(Oryza sativa[15]有60个、玉米(Zea mays[16]有86个、大白菜(Brassica rapa ssp. pekinensis[17]有48个、毛果杨(Populus trichocarpa[18]有106个、中国蔷薇(Rosa chinensis[19]有56个成员,大戟科的木薯(Manihot esculenta[20]有77个、麻风树(Jatropha curcas[21]和蓖麻(Castor bean[22]均有48个成员。
GRAS基因家族在植物生长发育、激素信号传导、逆境响应等多个生物学过程中发挥着重要的调控作用。如GRAS家族成员DELLA蛋白作为赤霉素(gibberellin,GA)信号转导途径的负调控因子,通过与其他蛋白互作从而介导GA调控植物生长[23]。此外,DELLA还参与调控茉莉酸(jasmonic acid,JA)信号转导[24]及次生细胞壁形成[25-26];PAT1作为光敏色素A信号途径的正调控因子参与光信号途径调控[27];HAM参与茎尖分生组织的生长发育[28];SCR和SHR通过形成复合体进而共同调控拟南芥根和芽的径向生长[29];SCL3参与调控陆地棉根的伸长[30];在大豆中过表达GmGRAS37基因可以增强植株的耐旱和耐盐能力[31]。近年来,随着对GRAS基因的深入研究,越来越多的证据表明,GRAS基因家族在植物的适应性进化和环境适应性方面起着关键的作用[32-34]
巴西橡胶树(Hevea brasiliensis),简称橡胶树,原产于巴西亚马逊河流域马拉岳西部地区,是大戟科橡胶树属一种典型的热带雨林树种,也是我国及世界热区的一种重要经济作物。橡胶树所产生的胶乳是天然橡胶的主要原料。天然橡胶是重要的战略物资和工业原料,尽管世界上有2000多种产胶植物,如银胶菊[35]、橡胶草[36]和杜仲[37]等,但目前所使用的天然橡胶约98%仍来源于橡胶树[38]。随着橡胶树全基因组测序工作的完成,为基因家族的全基因组分析提供了便利,也为橡胶树功能基因组学研究提供了可靠的基因组数据信息[39-41]。基于GRAS基因家族在植物生长发育和逆境胁迫响应中的重要作用,本研究利用生物信息学方法,以橡胶树基因组为基础,鉴定橡胶树GRAS基因家族成员,并对其系统进化、基因结构、染色体位置和启动子顺式作用元件等进行分析,利用转录组数据及qPCR技术分析GRAS基因表达模式,从而为橡胶树GRAS基因功能的解析提供理论依据。
本研究所采用的试验材料均来自于中国热带农业科学院试验场(海南省儋州市)种植的橡胶树(Hevea brasiliensis)热研73397品种。采集橡胶树不同组织(雌花、雄花、木质部、叶片、树皮和胶乳),不同节间木质部(选取橡胶树顶端分生组织从上往下数第一、第三和第五节间木质部),以及150 mg/L外源GA3处理21周后(每周喷洒处理1次)的橡胶树幼苗的木质部(以H2O处理作为对照)样品,立即置于液氮中,带回实验室后于–80 ℃中保存备用。每5株树为1个生物学重复,每个样品3个生物学重复。
从NCBI数据库(https://www.ncbi.nlm.nih.gov/)中下载橡胶树基因组序列、蛋白质序列和注释信息。利用Pfam数据库(http://pfam-legacy.xfam.org/)下载的GRAS结构域(PF03514)和隐马尔可夫模型(HMM)文件,通过hmmer 3.0软件筛选橡胶树基因组数据库中含有GRAS结构域的全部蛋白序列,选取e值小于1e–5的候选蛋白序列。使用ClustalX 2.1软件将候选蛋白序列进行一一比对去除冗余,并通过SMART(https://smart.embl.de/)和NCBI-CDD数据库(https://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml)鉴定其保守结构域,去除不含GRAS结构域的序列,得到橡胶树GRAS家族成员。分别利用ExPASy ProtParam(https://web.expasy.org/protparam/)和Plant-mPLoc(http://www.csbio.sjtu.edu.cn/bioinf/plant-multi/)在线软件进行氨基酸长度、分子量大小、等电点、疏水性等理化性质和亚细胞定位预测。
通过PlantTFdb(http://planttfdb.gao-lab.org/index.php)数据库和NCBI数据库下载拟南芥、毛果杨和水稻GRAS家族蛋白序列,并与橡胶树GRAS蛋白序列进行多序列比对。利用MEGA 11软件,采用邻接法(neighbor-joining method,NJ)构建系统进化树,bootstrap设置为1000以测试进化树的可靠性。利用Evolview(https://www.evolgenius.info/evolviewv2/#login)在线软件和AI软件进行结果美化。
根据橡胶树基因组注释信息,利用在线网站MEME(https://meme-suite.org/meme/)与NCBI Batch CD-search(https://www.ncbi.nlm.nih.gov/Structure/bwrpsb/bwrpsb.cgi)在线软件进行motif预测和保守结构域分析,其中motif数量设置为10,其他参数均为默认值。通过使用TBtools软件对橡胶树GRAS家族的外显子-内含子结构进行分析,并将系统进化树、蛋白保守基序、保守结构域和基因结构进行可视化展示。
利用TBtools软件在橡胶树基因组注释信息的基础上,将橡胶树GRAS基因定位到染色体上,并作共线性分析,同时利用该软件计算其Ka/Ks值。
选取橡胶树GRAS转录起始位点上游2000 bp的序列作为启动子分析区域,利用PlantCARE(https://bioinformatics.psb.ugent.be/webtools/plantcare/html/)在线软件进行启动子顺式作用元件预测,并通过TBtools进行可视化展示。
利用课题组前期获得的RNA-Seq数据,以及Hevea DB(http://hevea.catas.cn/home/index)数据库中公布的转录数据,获得不同组织(胶乳、树皮、叶片、雌花、雄花和木质部)及叶片不同发育时期(古铜期、变色期、淡绿期和稳定期)的橡胶树GRAS家族成员的转录本FPKM(fragments per kilobase of exon per million reads mapped)值,并使用TBtools软件对橡胶树GRAS基因表达水平进行聚类及热图绘制。
对橡胶树DELLA亚家族6个成员组织的转录组表达数据进行qPCR验证,并分析其在不同节间木质部及GA3处理下的表达模式。利用天根生化科技(北京)有限公司的RNAprep Pure多糖多酚植物总RNA提取试剂盒(TIANGEN,Beijing,China)提取样品总RNA。采用NanoDrop 2000分光光度计和凝胶电泳检测RNA样品的浓度和完整性。将1 μg RNA样品用PrimeScriptTM RT reagent Kit with gDNA Eraser试剂盒(Takara,Dalian,China)反转录为cDNA。采用Primer 3软件设计HbGRAS基因的qPCR引物(表1),以YLS8为内参基因。将上述反转录得到的cDNA作为模板,利用2×Q3 SYBR qPCR Master Mix(Universal)(TOLOBIO,China)进行qPCR,反应体系与扩增程序按照说明书进行。采用2–ΔΔCT法计算基因的相对表达水平。本实验包括3个生物学重复和3个技术重复。
根据NCBI数据库中下载的橡胶树蛋白质序列及隐马尔可夫模型,结合SMART和NCBI-CDD数据库筛选和验证,最终得到91个非冗余的橡胶树GRAS基因家族成员,根据其在染色上的位置将其命名为HbGRAS1~HbGRAS91表2)。理化性质分析结果显示,橡胶树GRAS基因编码的蛋白长度在117~824个氨基酸之间,其中HbGRAS91的氨基酸序列最短,HbGRAS9最长。蛋白分子量在14.07~89.46 kDa之间,等电点在4.72(HbGRAS 70)~9.07(HbGRAS21)之间,平均值为6.90。蛋白总平均疏水性在–0.656~0.151之间,其中,除HbGRAS12、HbGRAS32、HbGRAS59和HbGRAS61的总平均疏水性大于0之外,其余皆小于0,说明橡胶树GRAS家族成员大部分为亲水蛋白。蛋白亚细胞定位预测结果显示,有49个HbGRAS蛋白定位于细胞核,36个定位于叶绿体,3个定位于质膜,2个定位于细胞质,1个定位于过氧化物酶体。
为解析橡胶树GRAS蛋白的特征,分别从PlantTFdb和NCBI数据库中下载拟南芥、毛果杨和水稻GRAS家族蛋白序列,与本研究鉴定得到的91个橡胶树GRAS家族成员的蛋白序列进行比对及系统进化分析。结果表明,GRAS蛋白被划分为14个亚家族,分别是Os19、HAM、SCL4/7、LAS、SCR、DLT、SCL3、Os4、Os43、DELLA、Pt20、LISCL、SHR和PAT1(图1)。其中LISCL亚家族的成员数目最多有16个,PAT1亚家族有13个,HAM亚家族有11个,SHR亚家族有10个,Pt20亚家族有8个,Os4、SCR和DELLA亚家族各有6个,SCL3亚家族有5个,Os19、Os43、SCL4/7、LAS和DLT各亚家族仅有2个成员。比较不同植物之间GRAS各亚家族的数量发现,橡胶树、拟南芥和水稻中LISCL亚家族的数量最多,分别为16、7和10个。毛果杨中DELLA和HAM亚家族成员数量最多,均为14个。Pt20亚家族仅存在于橡胶树和毛果杨中,而拟南芥无Os4、Os43和Os19亚家族成员(表3图2A)。
保守基序分析发现,大多数motifs位于序列C端,motif 6存在于全部HbGRAS蛋白中,且始终在C端。motif 1大多与motif 4、motif 5或者motif 10相邻。同一亚族的HbGRAS成员通常具有相似的基序组成。例如,LISCL亚族除HbGRAS91只含有motif 2和motif 6外,其余均包括motif 9、motif 7、motif 1、motif 8、motif 5、motif 3、motif 2、motif 6,DELLA亚族均含有motif 9、motif 7、motif 4、motif 1、motif 10、motif 3、motif 2、motif 6,HAM亚家族成员仅含有4个保守的motifs(图2B)。
保守结构域分析结果显示,HbGRAS成员均含有GRAS或GRAS superfamily结构域,除HbGRAS91外其他均位于C端,而DELLA结构域仅存在于DELLA亚家族中。同一亚家族的成员其基因结构相似,如PAT1亚家族仅有GRAS结构域,Pt20亚家族仅有GRAS superfamily结构域。DELLA亚家族中除HbGRAS62外,其余均含有DELLA保守结构域(图2C)。
基因结构多样性是基因家族进化的重要组成部分[42]。橡胶树GRAS基因具有0~7个数量不等的内含子,其中63个HbGRAS无内含子,18个HbGRAS仅有1个内含子,HbGRAS59含有7个内含子,数量最多。DELLA、LAS、Os19、HAM和DLT亚家族无内含子,Os4/7、SCL3和SHR亚家族含有0~1个内含子,Os4亚家族含有0~7个内含子(图2D)。总体来说,系统进化中同一亚家族的橡胶树GRAS基因具有相似的外显子-内含子结构。
橡胶树GRAS基因的染色体定位如图3所示,91个HbGRAS基因分布于除11号染色体外的其他17条染色体和2条Scaffold上,并且每个染色体上分布的数目不同。16号染色体上分布最多,有17个基因,约占总数的18.68%,其次是9号染色体分布有12个基因,而8和18号染色体,以及Scaffold402和Scaffold409分布最少,各自仅含1个HbGRAS基因。
串联重复事件是指200 kb内包含2个或更多基因的染色体区[43],在基因组进化、调控和稳定性等方面具有重要的作用[44]。在橡胶树4、9、15和16号等4条染色体上共发现17个HbGRAS基因的10个串联重复事件(图3)。共线性分析显示,橡胶树GRAS基因片段重复区域中发现了87个基因(图4),说明片段重复事件可能是橡胶树GRAS基因家族成员进化的主要原因。HbGRAS家族的同源基因对的Ka/Ks值在0.091~0.388之间,说明这些基因经过片段复制后发生了纯化选择。
启动子区顺式作用元件分析结果显示,橡胶树GRAS家族主要包含植物激素应答顺式作用元件,如GA、茉莉酸甲酯(methyl jasmonate,MeJA)、脱落酸(abscisic acid,ABA)、生长素(auxin)和水杨酸(salicylic acid,SA)响应元件,胁迫应答顺式作用元件,如伤害、干旱和低温响应元件,以及参与分生组织、胚乳、种子等时空表达及光响应的顺式作用元件等。其中,光响应元件在全部91个HbGRAS基因中都存在且数量最多,有1111个。其次,是茉莉酸甲酯响应元件有178个,厌氧诱导元件164个,脱落酸响应元件129个,GA响应元件85个,其中数量最少的元件是光敏色素互作因子、SEF1因子结合位点和参与栅栏叶肉细胞分化的顺式作用元件,各有2个(图5)。上述结果表明,HbGRAS可能参与多种植物激素和环境胁迫应答,在植物生长发育和逆境胁迫响应中起着重要作用。
HbGRAS基因在橡胶树胶乳、树皮、叶片、雌花、雄花和木质部等不同组织的表达模式如图6所示,其中HbGRAS11HbGRAS12HbGRAS26HbGRAS30HbGRAS42HbGRAS48HbGRAS49HbGRAS59HbGRAS69等9个基因在所有检测组织中均不表达。HbGRAS45HbGRAS84在胶乳中高表达,HbGRAS67在树皮和木质部中表达量较高,HbGRAS82在叶片和木质部中的表达丰度较高。雄花中表达丰度最高的是HbGRAS60,其次是HbGRAS87。不同亚族中HbGRAS的组织表达模式也不尽相同,比如LAS和Pt20亚家族成员在所有组织中的表达水平都低于其他亚家族,而PAT1、DELLA和SCL4/7亚家族的相对表达量较其他各亚族略高。
为进一步了解HbGRAS在橡胶树叶片发育中的作用,从Hevea DB数据库下载HbGRAS基因在橡胶树叶片不同发育时期的转录组数据,表达模式分析结果显示,DELLA亚家族中HbGRAS44随着叶片的发育进程表达量逐渐上调,而HbGRAS58HbGRAS64、HbGRAS82HbGRAS89则逐渐下调表达;PAT1亚家族中HbGRAS7HbGRAS60,HAM亚家族中HbGRAS6HbGRAS36均随着叶片的成熟表达量逐渐上调。HAM亚族中HbGRAS84HbGRAS54在变色期和淡绿期的表达量相对较高(图7),说明HbGRAS基因表达与叶片发育有关,但可能存在功能差异。
作为GRAS家族的重要成员,DELLA是GA信号传导途径的负调控因子,在植物生长发育过程中发挥重要作用[45]。因此,进一步利用qPCR技术分析橡胶树DELLA亚家族成员的基因表达模式。结果显示HbGRAS62在树皮中表达量最高,木质部中表达量最低,而RNA-Seq结果显示表达量最高和最低的组织分别为胶乳和雌花。其余5个DELLA基因表达量最高和最低的组织均与RNA-seq结果一致,其中HbGRAS44分别为叶片和树皮、HbGRAS58分别为叶片和胶乳、HbGRAS64分别为雌花和胶乳、HbGRAS82HbGRAS89均分别为木质部和胶乳(图8)。造成HbGRAS62 qPCR和RNA-Seq表达模式不一致的原因可能与2种技术本身的差异(即转录组测序是对该基因的所有转录本定量,而qPCR则可能不能代表所有的转录本)有关。在不同节间木质部中,除HbGRAS62外,其余5个橡胶树DELLA基因均随木质化程度加深上调表达(图9),说明橡胶树DELLA基因可能参与橡胶树茎的次生细胞壁形成。外源GA3处理抑制DELLA亚家族成员表达(图10),说明DELLA基因表达受GA调控。
GRAS作为植物中特有的一类转录因子,在植物的生长发育以及非生物胁迫应答中具有重要的调控作用,但目前在橡胶树中尚无该转录因子家族分析相关的研究报道。本研究从橡胶树全基因组中筛选并鉴定到HbGRAS基因家族成员91个,所有HbGRAS蛋白在结构上存在显著差异,表明其高度复杂。其成员数量与拟南芥(33个)、水稻(60个)、玉米(86个)、葡萄(43个)、辣椒(50个)[46]、杨树(106个)、苹果(127个)[47]等物种相比差异较大,较同科的木薯(77个)、蓖麻(48个)和麻风树(48个)中GRAS基因数量明显增加,且蛋白长度在117~824个氨基酸之间变化,这种较大的差异可能与基因组大小或基因复制事件有关[20]。系统进化分析显示,HbGRAS蛋白可分为14个亚家族,而在水稻的每个亚群中均鉴定到HbGRAS蛋白,这表明GRAS家族的分化可能早于单、双子叶植物的分化。橡胶树GRAS亚族数量与木薯一致[20],其中LISCL成员最多(16个,17.58%),与拟南芥和水稻等植物相似[15],表明这些GRAS基因家族在长期进化过程中可能具有较强的分化能力。基于系统进化关系和多序列比对结果,发现大多数HbGRAS蛋白的N端包含1个高度无序的区域,这导致了GRAS蛋白的多样化,并影响了其功能分化。DELLA亚家族蛋白N端相对保守。橡胶树DELLA亚家族成员中除HbGRAS62无DELLA保守结构域外,其余5个均含有DELLA结构域,这可能是HbGRAS62在进化过程中发生了DELLA基因的丢失事件,或者该基因不包含典型的“DELLA”和“DXLLX”五肽结构而导致[48]
分析91个HbGRAS基因的内含子和外显子结构发现,无内含子的HbGRAS基因比例(69.23%)与同科的木薯(53.25%)[20]、蓖麻(78.3%)[22]和麻风树(95.83%)[21]类似,均较高。内含子可以增加基因长度及重组频率,有利于物种进化[49]。虽然内含子较少的基因在物种进化或重组中没有优势,但它们往往对压力反应迅速[50]。因此,推测许多橡胶树GRAS基因成员可能会对环境变化做出快速响应。
基因扩增是基因组进化的重要驱动力,可以导致新的功能基因的产生和新物种的分化,从而使植物在进化过程中更好地适应环境[17]。染色体定位结果显示,HbGRAS基因位于除Chr11外的几乎所有染色体上,这可能是进化过程中发生片段丢失或染色体移位导致。同时,发现有17个HbGRAS基因(18.68%)发生串联重复事件,所有具有串联重复序列的HbGRAS基因均来自同一亚家族,且主要集中在LISCL亚家族中(58.82%)。这意味着,基因复制保留在全基因组复制后存在一定程度的偏倚,不同亚家族的保留和丢失也不同。另外,有研究发现,如果蛋白质与基因编码的其他产物存在相互作用,则在复制事件发生后,这类基因会发生偏置[51]。共线性分析显示,片段重复区域中有87个HbGRAS基因(95.6%),说明片段重复在橡胶树GRAS基因进化中可能发挥主要作用。
GA促进植物次生细胞壁形成[52],DELLA通过与相关转录因子互作调控水稻次生细胞壁中纤维素合成[53]。外施GA3抑制橡胶树木质部DELLA表达,DELLA亚家族成员HbGRAS82HbGRAS89在木质部中高表达,且随橡胶树木质化程度加深上调表达,故推测它们可能参与橡胶树次生细胞壁的形成。拟南芥DELLA蛋白竞争性地阻止阻遏蛋白JAZ与转录因子MYC2结合,从而提高MYC2对靶基因的调控能力[54];WILD等[55]证实拟南芥RGL3能分别与MYC2和JAZ蛋白互作,进而调控JA介导的响应;MYC2是调控橡胶生物合成途径之一——JA信号途径的关键因子。吴绍华等[56]发现割胶和MeJA调控橡胶树HbGAIPB基因的表达。本研究结果显示橡胶树DELLA亚族成员在胶乳中均有表达,且除HbGRAS44外其他成员都含有MeJA响应元件。据此,推测橡胶树DELLA基因可能通过调控JA信号途径参与橡胶生物合成。以上结果为进一步研究橡胶树GRAS基因的生物学功能、调控橡胶树生长发育与逆境响应的分子机制奠定了一定的理论基础。
  • 海南省自然科学基金高层次人才项目(321RC654)
  • 海南省科技人才创新项目(KJRC2023C18)
  • 海南省自然科学基金青年基金项目(322QN409)
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2024年第45卷第9期
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doi: 10.3969/j.issn.1000-2561.2024.09.001
  • 接收时间:2023-02-18
  • 首发时间:2026-06-23
  • 出版时间:2024-09-25
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  • 收稿日期:2023-02-18
  • 修回日期:2023-03-20
基金
海南省自然科学基金高层次人才项目(321RC654)
海南省科技人才创新项目(KJRC2023C18)
海南省自然科学基金青年基金项目(322QN409)
作者信息
    1.浙江农林大学现代农学院,浙江杭州 311300
    2.中国热带农业科学院橡胶研究所/热带作物生物育种全国重点实验室,海南海口 571101
    3.中国热带农业科学院三亚研究院,海南三亚 572025

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* 邓治(DENG Zhi),E-mail:
程汉(CHENG Han),E-mail:
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2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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