Clough Steven J, Tuteja Jigyasa H, Li Min, Marek Laura F, Shoemaker Randy C, Vodkin Lila O
USDA-ARS and the Department of Crop Science, University of Illinois, Urbana, IL 61801, USA.
Genome. 2004 Oct;47(5):819-31. doi: 10.1139/g04-049.
The I locus in soybean (Glycine max) corresponds to a region of chalcone synthase (CHS) gene duplications affecting seed pigmentation. We sequenced and annotated BAC clone 104J7, which harbors a dominant i(i) allele from Glycine max 'Williams 82', to gain insight into the genetic structure of this multigenic region in addition to examining its flanking regions. The 103-kb BAC encompasses a gene-rich region with 11 putatively expressed genes. In addition to six copies of CHS, these genes include: a geranylgeranyltransferase type II beta subunit (E.C.2.5.1.60), a beta-galactosidase, a putative spermine and (or) spermidine synthase (E.C.2.5.1.16), and an unknown expressed gene. Strikingly, sequencing data revealed that the 10.91-kb CHS1, CHS3, CHS4 cluster is present as a perfect inverted repeat separated by 5.87 kb. Contiguous arrangement of CHS paralogs could lead to folding into multiple secondary structures, hypothesized to induce deletions that have previously been shown to effect CHS expression. BAC104J7 also contains several gene fragments representing a cation/hydrogen exchanger, a 40S ribosomal protein, a CBL-interacting protein kinase, and the amino terminus of a subtilisin. Chimeric ESTs were identified that may represent read-through transcription from a flanking truncated gene into a CHS cluster, generating aberrant CHS RNA molecules that could play a role in CHS gene silencing.
大豆(Glycine max)中的I基因座对应于查尔酮合酶(CHS)基因重复区域,该区域影响种子色素沉着。我们对BAC克隆104J7进行了测序和注释,该克隆含有来自大豆‘Williams 82’的显性i(i)等位基因,以深入了解这个多基因区域的遗传结构,并研究其侧翼区域。这个103 kb的BAC包含一个基因丰富的区域,有11个推定的表达基因。除了6个CHS拷贝外,这些基因还包括:一个II型香叶基香叶基转移酶β亚基(E.C.2.5.1.60)、一个β-半乳糖苷酶、一个推定的精胺和(或)亚精胺合酶(E.C.2.5.1.16),以及一个未知的表达基因。引人注目的是,测序数据显示,10.91 kb的CHS1、CHS3、CHS4簇以一个完美的反向重复形式存在,中间间隔5.87 kb。CHS旁系同源物的连续排列可能导致折叠成多个二级结构,据推测会诱导缺失,而这些缺失先前已被证明会影响CHS表达。BAC104J7还包含几个基因片段,分别代表一个阳离子/氢交换体、一个40S核糖体蛋白、一个CBL相互作用蛋白激酶,以及一个枯草杆菌蛋白酶的氨基末端。我们鉴定出了嵌合EST,它们可能代表从侧翼截短基因到CHS簇的通读转录,产生异常的CHS RNA分子,这些分子可能在CHS基因沉默中发挥作用。