A BAC Contig Map of the Ly49 Gene Cluster in 129 Mice Reveals Extensive Differences in Gene Content Relative to C57BL/6 Mice

Genomics ◽  
2002 ◽  
Vol 79 (3) ◽  
pp. 437-444 ◽  
Author(s):  
Andrew P Makrigiannis ◽  
Amanda T Pau ◽  
Pamela L Schwartzberg ◽  
Daniel W McVicar ◽  
Thomas W Beck ◽  
...  
2020 ◽  
Vol 12 (10) ◽  
pp. 1858-1868
Author(s):  
David Pizarro ◽  
Pradeep K Divakar ◽  
Felix Grewe ◽  
Ana Crespo ◽  
Francesco Dal Grande ◽  
...  

Abstract Lichen-forming fungi are known to produce a large number of secondary metabolites. Some metabolites are deposited in the cortical layer of the lichen thallus where they exert important ecological functions, such as UV filtering. The fact that closely related lineages of lichen-forming fungi can differ in cortical chemistry suggests that natural product biosynthesis in lichens can evolve independent from phylogenetic constraints. Usnic acid is one of the major cortical pigments in lichens. Here we used a comparative genomic approach on 46 lichen-forming fungal species of the Lecanoromycetes to elucidate the biosynthetic gene content and evolution of the gene cluster putatively responsible for the biosynthesis of usnic acid. Whole-genome sequences were gathered from taxa belonging to different orders and families of Lecanoromycetes, where Parmeliaceae is the most well-represented taxon, and analyzed with a variety of genomic tools. The highest number of biosynthetic gene clusters was found in Evernia prunastri, Pannoparmelia angustata, and Parmotrema austrosinense, respectively, and lowest in Canoparmelia nairobiensis, Bulbothrix sensibilis, and Hypotrachyna scytodes. We found that all studied species producing usnic acid contain the putative usnic acid biosynthetic gene cluster, whereas the cluster was absent in all genomes of species lacking usnic acid. The absence of the gene cluster was supported by an additional unsuccessful search for ß-ketoacylsynthase, the most conserved domain of the gene cluster, in the genomes of species lacking usnic acid. The domain architecture of this PKS cluster—homologous to the already known usnic acid PKS cluster (MPAS) and CYT450 (MPAO)—varies within the studied species, whereas the gene arrangement is highly similar in closely related taxa. We hypothesize that the ancestor of these lichen-forming fungi contained the putative usnic acid producing PKS cluster and that the gene cluster was lost repeatedly during the evolution of these groups. Our study provides insight into the genomic adaptations to the evolutionary success of these lichen-forming fungal species and sets a baseline for further exploration of biosynthetic gene content and its evolutionary significance.


Genomics ◽  
2001 ◽  
Vol 74 (2) ◽  
pp. 129-141 ◽  
Author(s):  
Joomyeong Kim ◽  
Laurie Gordon ◽  
Paramvir Dehal ◽  
Hummy Badri ◽  
Mari Christensen ◽  
...  

2003 ◽  
Vol 102 (1-4) ◽  
pp. 189-195 ◽  
Author(s):  
A.L. Gustafson ◽  
R.L. Tallmadge ◽  
N. Ramlachan ◽  
D. Miller ◽  
H. Bird ◽  
...  

1999 ◽  
Vol 9 (8) ◽  
pp. 763-774 ◽  
Author(s):  
Yicheng Cao ◽  
Hyung Lyun Kang ◽  
Xuequn Xu ◽  
Mei Wang ◽  
So Hee Dho ◽  
...  

We have constructed a complete coverage BAC contig map that spans a 12-Mb genomic segment in the human chromosome 16p13.1–p11.2 region. The map consists of 68 previously mapped STSs and 289 BAC clones, 51 of which—corresponding to a total of 7.721 Mb of genomic DNA—have been sequenced, and provides a high resolution physical map of the region. Contigs were initially built based mainly on the analysis of STS contents and restriction fingerprint patterns of the clones. To close the gaps, probes derived from BAC clone ends were used to screen deeper BAC libraries. Clone end sequence data obtained from chromosome 16-specific BACs, as well as from public databases, were used for the identification of BACs that overlap with fully sequenced BACs by means of sequence match. This approach allowed precise alignment of clone overlaps in addition to restriction fingerprint comparison. A freehand contig drawing software tool was developed and used to manage the map data graphically and generate a real scale physical map. The map we present here is ∼3.5 × deep and provides a minimal tiling path that covers the region in an array of contigous, overlapping BACs.


2008 ◽  
Vol 120 (1-2) ◽  
pp. 164-172 ◽  
Author(s):  
C. Brinkmeyer-Langford ◽  
T. Raudsepp ◽  
A. Gustafson-Seabury ◽  
B.P. Chowdhary
Keyword(s):  

1999 ◽  
Vol 9 (8) ◽  
pp. 732-738 ◽  
Author(s):  
Andreas Lengeling ◽  
Tim Wiltshire ◽  
Chris Otmani ◽  
Maja Bućan

The type-A receptors for the neurotransmitter GABA (γ-aminobutyric acid) are ligand-gated chloride channels that mediate postsynaptic inhibition. The functional diversity of these receptors comes from the use of a large repertoire of subunits encoded by separate genes, as well as from differences in subunit composition of individual receptors. In mammals, a majority of GABAAreceptor subunit genes are located in gene clusters that may be important for their regulated expression and function. We have established a high-resolution physical map of the cluster of genes encoding GABAA receptor subunits α2 (Gabra2), β1 (Gabrb1), and γ1 (Gabrg1) on mouse chromosome 5. Rat cDNA probes and specific sequence probes for all three GABAA receptor subunit genes have been used to initiate the construction of a sequence-ready contig of bacterial artificial chromosomes (BACs) encompassing this cluster. In the process of contig construction clones from 129/Sv and C57BL/6J BAC libraries were isolated. The assembled 1.3-Mb contig, consisting of 45 BACs, gives five- to sixfold coverage over the gene cluster and provides an average resolution of one marker every 32 kb. A number of BAC insert ends were sequenced, generating 30 new sequence tag sites (STS) in addition to 6 Gabr gene-based and 3 expressed sequence tag (EST)-based markers. STSs from, and surrounding, theGabrg1–Gabra2–Gabrb1 gene cluster were mapped in the T31 mouse radiation hybrid panel. The integration of the BAC contig with a map of loci ordered by radiation hybrid mapping suggested the most likely genomic orientation of this cluster on mouse chromosome 5: cen–D5Mit151–Gabrg1–Gabra2–Gabrb1–D5Mit58–tel. This established contig will serve as a template for genomic sequencing and for functional analysis of the GABAA gene cluster on mouse chromosome 5 and the corresponding region on human chromosome 4.The sequence data described in this paper have been submitted to the GenBank/GSS data libraries under accession nos.AF156490 and AQ589406–AQ589436.


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