UMR INRA/ENVT Laboratoire de Génétique Cellulaire, INRA, Castanet-Tolosan, 31326, France.
BMC Genomics. 2010 Nov 4;11:616. doi: 10.1186/1471-2164-11-616.
The chicken karyotype is composed of 39 chromosome pairs, of which 9 still remain totally absent from the current genome sequence assembly, despite international efforts towards complete coverage. Some others are only very partially sequenced, amongst which microchromosome 16 (GGA16), particularly under-represented, with only 433 kb assembled for a full estimated size of 9 to 11 Mb. Besides the obvious need of full genome coverage with genetic markers for QTL (Quantitative Trait Loci) mapping and major genes identification studies, there is a major interest in the detailed study of this chromosome because it carries the two genetically independent MHC complexes B and Y. In addition, GGA16 carries the ribosomal RNA (rRNA) genes cluster, also known as the NOR (nucleolus organizer region). The purpose of the present study is to construct and present high resolution integrated maps of GGA16 to refine its organization and improve its coverage with genetic markers.
We developed 79 STS (Sequence Tagged Site) markers to build a physical RH (radiation hybrid) map and 34 genetic markers to extend the genetic map of GGA16. We screened a BAC (Bacterial Artificial Chromosome) library with markers for the MHC-B, MHC-Y and rRNA complexes. Selected clones were used to perform high resolution FISH (Fluorescent In Situ Hybridization) mapping on giant meiotic lampbrush chromosomes, allowing meiotic mapping in addition to the confirmation of the order of the three clusters along the chromosome. A region with high recombination rates and containing PO41 repeated elements separates the two MHC complexes.
The three complementary mapping strategies used refine greatly our knowledge of chicken microchromosome 16 organisation. The characterisation of the recombination hotspots separating the two MHC complexes demonstrates the presence of PO41 repetitive sequences both in tandem and inverted orientation. However, this region still needs to be studied in more detail.
鸡的染色体组由 39 对染色体组成,尽管国际上努力实现完全覆盖,但目前的基因组序列组装中仍完全缺失其中 9 对。还有一些染色体只进行了非常部分的测序,其中微染色体 16(GGA16)尤其代表性不足,估计全长 9 到 11Mb,仅组装了 433kb。除了需要用遗传标记进行 QTL(数量性状基因座)作图和主要基因鉴定研究来实现全基因组覆盖之外,人们对这条染色体进行详细研究也很感兴趣,因为它携带两个遗传上独立的 MHC 复合物 B 和 Y。此外,GGA16 还携带核糖体 RNA(rRNA)基因簇,也称为 NOR(核仁组织者区域)。本研究的目的是构建和呈现 GGA16 的高分辨率整合图谱,以细化其结构并提高其遗传标记的覆盖度。
我们开发了 79 个 STS(序列标记位点)标记来构建物理 RH(辐射杂种)图谱,以及 34 个遗传标记来扩展 GGA16 的遗传图谱。我们用 MHC-B、MHC-Y 和 rRNA 复合物的标记筛选了一个 BAC(细菌人工染色体)文库。选择的克隆用于在巨大的减数分裂灯刷染色体上进行高分辨率 FISH(荧光原位杂交)作图,除了确认三个簇在染色体上的顺序外,还允许进行减数分裂作图。一个包含 PO41 重复元件的高重组率区域将两个 MHC 复合物分开。
使用的三种互补作图策略极大地改进了我们对鸡微染色体 16 组织的认识。分离两个 MHC 复合物的重组热点的特征表明,PO41 重复序列以串联和反向取向存在。然而,这个区域仍需要更详细地研究。