华北农学报
華北農學報
화북농학보
ACTA AGRICULTURAE BOREALI-SINICA
2014年
4期
32-36
,共5页
于月华%张跃强%海热古力·阿不力孜%刘真芳%梁小莉
于月華%張躍彊%海熱古力·阿不力孜%劉真芳%樑小莉
우월화%장약강%해열고력·아불력자%류진방%량소리
小麦%TaMSR基因%表达分析%染色体定位
小麥%TaMSR基因%錶達分析%染色體定位
소맥%TaMSR기인%표체분석%염색체정위
Wheat%TaMSR gene%Expression analysis%Chromosomal localization
为了发掘小麦育性基因,采用同源克隆的方法,从小麦花药中克隆了3个与拟南芥AtMS2和水稻OsMS2基因同源的cDNA序列。TaMSR-1、TaMSR-2和TaMSR-3分别具有1842,1824,1830 bp 的开放阅读框,各自编码613,607,609个氨基酸。推导的蛋白质序列中包含2个保守区:NAD_binding 和Sterile保守功能域。氨基酸序列分析发现,TaMSR与水稻OsMSR2和拟南芥AtMSR2具有较高的相似性。采用基因特异定位引物PCR技术对中国春缺失系材料进行扩增,将TaMSR-1、TaMSR-2和TaMSR-3基因分别定位于4AS、4DL和4BL染色体上。半定量RT-PCR分析表明,TaMSR基因是花药组织特异表达的基因。这些结果说明,TaMSR基因可能在小麦花药发育过程中起重要作用。
為瞭髮掘小麥育性基因,採用同源剋隆的方法,從小麥花藥中剋隆瞭3箇與擬南芥AtMS2和水稻OsMS2基因同源的cDNA序列。TaMSR-1、TaMSR-2和TaMSR-3分彆具有1842,1824,1830 bp 的開放閱讀框,各自編碼613,607,609箇氨基痠。推導的蛋白質序列中包含2箇保守區:NAD_binding 和Sterile保守功能域。氨基痠序列分析髮現,TaMSR與水稻OsMSR2和擬南芥AtMSR2具有較高的相似性。採用基因特異定位引物PCR技術對中國春缺失繫材料進行擴增,將TaMSR-1、TaMSR-2和TaMSR-3基因分彆定位于4AS、4DL和4BL染色體上。半定量RT-PCR分析錶明,TaMSR基因是花藥組織特異錶達的基因。這些結果說明,TaMSR基因可能在小麥花藥髮育過程中起重要作用。
위료발굴소맥육성기인,채용동원극륭적방법,종소맥화약중극륭료3개여의남개AtMS2화수도OsMS2기인동원적cDNA서렬。TaMSR-1、TaMSR-2화TaMSR-3분별구유1842,1824,1830 bp 적개방열독광,각자편마613,607,609개안기산。추도적단백질서렬중포함2개보수구:NAD_binding 화Sterile보수공능역。안기산서렬분석발현,TaMSR여수도OsMSR2화의남개AtMSR2구유교고적상사성。채용기인특이정위인물PCR기술대중국춘결실계재료진행확증,장TaMSR-1、TaMSR-2화TaMSR-3기인분별정위우4AS、4DL화4BL염색체상。반정량RT-PCR분석표명,TaMSR기인시화약조직특이표체적기인。저사결과설명,TaMSR기인가능재소맥화약발육과정중기중요작용。
In search for fertility gene in wheat , three cDNAs that homologous to AtMS2 and putative OsMS2 , designated as TaMSR-1 ,TaMSR-2 and TaMSR-3 were cloned from wheat anther by homologogy-based cloning ap-proach .TaMSR-1 ,TaMSR-2 and TaMSR-3 contain open reading frames of 1 842 ,1 824 ,1 830 bp encoding proteins of 613 ,607 ,609 amino acid residues including two male sterile conserved domains:NAD-binding domain and male sterile C-terminal domain , respectively .The deduced amino acid sequence of TaMSR had high similarities with OsMSR2 and AtMSR2.Using Chinese_Spring_Deletion line,TaMSR-1,TaMSR-2 and TaMSR-3 genes were located on chromosome 4AS,4DL and 4BL,respectively.Semi-quantitative RT-PCR analysis revealed that TaMSR gene was anther specific expressed gene .These results suggested that TaMSR may plays an important role in wheat anther de-velopment .