山东农业科学
山東農業科學
산동농업과학
Shandong Agricultural Sciences
2015年
11期
12-17
,共6页
吕广德%高明刚%李洪娜%郭营%李斯深
呂廣德%高明剛%李洪娜%郭營%李斯深
려엄덕%고명강%리홍나%곽영%리사심
普通小麦%TaPAPA1%锌指蛋白%SNP位点%标记开发%连锁分析
普通小麥%TaPAPA1%鋅指蛋白%SNP位點%標記開髮%連鎖分析
보통소맥%TaPAPA1%자지단백%SNP위점%표기개발%련쇄분석
Wheat (Triticum aestivum L.)%TaPAPA1%Zf -HIT protein%SNP site%Marker develop-ment%Linkage analysis
研究发现锌指(Zinc-finger HIT,Zf-HIT)蛋白在植物的抗逆性方面有重要的调控作用。本研究从普通小麦中克隆到一个含有 PAPA -1-like[Pim -1-associated protein -1(PAP -1)-associated protein -1-like]和 Zf -HIT 结构域的蛋白质基因,命名为 TaPAPA1。通过测序和序列分析,得到三条 gDNA 和三条cDNA 序列,均包含6个外显子和5个内含子。根据序列间的差异位点设计基因组特异引物,用中国春小麦缺体—四体系将该基因定位在小麦第五同源群。TaPAPA1-5A、TaPAPA1-5B 和 TaPAPA1-5D 的编码序列长度分别为1473、1473 bp 和1470 bp,分别编码490、490和489个氨基酸。在5B 染色体检测到该基因的一个 SNP 位点,并开发 AS -PCR 标记 TaPAPA1-5B -AS1/2。利用 RIL(Recombinant inbred line)群体,把该标记定位在 D -1207571和 D -1100783之间,遗传距离分别是0.51 cM和0.71 cM。
研究髮現鋅指(Zinc-finger HIT,Zf-HIT)蛋白在植物的抗逆性方麵有重要的調控作用。本研究從普通小麥中剋隆到一箇含有 PAPA -1-like[Pim -1-associated protein -1(PAP -1)-associated protein -1-like]和 Zf -HIT 結構域的蛋白質基因,命名為 TaPAPA1。通過測序和序列分析,得到三條 gDNA 和三條cDNA 序列,均包含6箇外顯子和5箇內含子。根據序列間的差異位點設計基因組特異引物,用中國春小麥缺體—四體繫將該基因定位在小麥第五同源群。TaPAPA1-5A、TaPAPA1-5B 和 TaPAPA1-5D 的編碼序列長度分彆為1473、1473 bp 和1470 bp,分彆編碼490、490和489箇氨基痠。在5B 染色體檢測到該基因的一箇 SNP 位點,併開髮 AS -PCR 標記 TaPAPA1-5B -AS1/2。利用 RIL(Recombinant inbred line)群體,把該標記定位在 D -1207571和 D -1100783之間,遺傳距離分彆是0.51 cM和0.71 cM。
연구발현자지(Zinc-finger HIT,Zf-HIT)단백재식물적항역성방면유중요적조공작용。본연구종보통소맥중극륭도일개함유 PAPA -1-like[Pim -1-associated protein -1(PAP -1)-associated protein -1-like]화 Zf -HIT 결구역적단백질기인,명명위 TaPAPA1。통과측서화서렬분석,득도삼조 gDNA 화삼조cDNA 서렬,균포함6개외현자화5개내함자。근거서렬간적차이위점설계기인조특이인물,용중국춘소맥결체—사체계장해기인정위재소맥제오동원군。TaPAPA1-5A、TaPAPA1-5B 화 TaPAPA1-5D 적편마서렬장도분별위1473、1473 bp 화1470 bp,분별편마490、490화489개안기산。재5B 염색체검측도해기인적일개 SNP 위점,병개발 AS -PCR 표기 TaPAPA1-5B -AS1/2。이용 RIL(Recombinant inbred line)군체,파해표기정위재 D -1207571화 D -1100783지간,유전거리분별시0.51 cM화0.71 cM。
Zinc -finger HIT protein plays an important role in the regulation of plant defense and stress response.In this study,a gene named TaPAPA1,who encoded one protein containing PAPA -1 -like [Pim -1 -associated protein -1 (PAP -1 )-associated protein -1 -like]and Zf -HIT (Zinc -finger HIT)domain, was cloned from wheat.Through sequence analysis,three cDNA and three gDNA sequences were got,which all had six exons and five introns.According to different sites among three gDNA sequences,three pairs of genome special primers were designed,and these genes were located in homologous group 5 using nullisomic -tetrasomic lines of Chinese Spring.The coding sequences of TaPAPA1 -5A,TaPAPA1 -5B and TaPAPA1 -5D were 1 473,1 473 bp and 1 470 bp,which encoded polypepetides with 490,490 and 489 amino acids,respectively. According to the SNP locus in TaPAPA1 -5B,the AS -PCR marker TaPAPA1 -5B -AS1 /2 was developed.U-sing a RIL (recombinant inbred line)population,the marker was located between marker D -1207571 and D -1100783 on 5B by linkage analysis with the genetic distance of 0.51 cMand 0.71 cM,respectively.