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Protein genes in repetitive sequence—antifreeze glycoproteins in Atlantic cod genome

Zhuang, Xuan, Yang, Chun, Fevolden, Svein-Erik, Cheng, C-H Christina·2012·BMC Genomics

Abstract

Background: Highly repetitive sequences are the bane of genome sequence assembly, and the short read lengths produced by current next generation sequencing technologies further exacerbates this obstacle. An adopted practice is to exclude repetitive sequences in genome data assembly, as the majority of repeats lack protein-coding genes. However, this could result in the exclusion of important genotypes in newly sequenced non-model species. The absence of the antifreeze glycoproteins (AFGP) gene family in the recently sequenced Atlantic cod genome serves as an example. Results: The Atlantic cod (Gadus morhua) genome was assembled entirely from Roche 454 short reads, demonstrating the feasibility of this approach. However, a well-known major adaptive trait, the AFGP, essential for survival in frigid Arctic marine habitats was absent in the annotated genome. To assess whether this resulted from population difference, we performed Southern blot analysis of genomic DNA from multiple individuals from the North East Arctic cod population that the sequenced cod belonged, and verified that the AFGP genotype is indeed present. We searched the raw assemblies of the Atlantic cod using our G. morhua AFGP gene, and located partial AFGP coding sequences in two sequence scaffolds. We found these two scaffolds constitute a partial genomic AFGP locus through comparative sequence analyses with our newly assembled genomic AFGP locus of the related polar cod, Boreogadus saida. By examining the sequence assembly and annotation methodologies used for the Atlantic cod genome, we deduced the primary cause of the absence of the AFGP gene family from the annotated genome was the removal of all repetitive Roche 454 short reads before sequence assembly, which would exclude most of the highly repetitive AFGP coding sequences. Secondarily, the model teleost genomes used in projection annotation of the Atlantic cod genome have no antifreeze trait, perpetuating the unawareness that the AFGP gene family is missing. Conclusions: We recovered some of the missing AFGP coding sequences and reconstructed a partial AFGP locus in the Atlantic cod genome, bringing to light that not all repetitive sequences lack protein coding information. Also, reliance on genomes of model organisms as reference for annotating protein-coding gene content of a newly sequenced non-model species could lead to omission of novel genetic traits.

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Figure 1 Southern blot analysis of Atlantic cod genomic DNA showing presence of AFGP coding sequences.TaqI digested genomic DNA (~10–15 μg) from Atlantic cod (lanes 1–14) and polar cod (lanes 15–17) hybridized strongly to a polar cod B. saida AFGP coding sequence probe. Atlantic cod individuals include Norwegian coastal cod (NCC) and North East Arctic cod (NEAC) from the Finnmark coast and marginal Barents Sea sites: (lanes 1–3) N69° 26.91′ E19° 37.56′; (lanes 4–5) N69° 58.34′ E30° 2.37′; (lanes 6–8) N70° 7.24′ E30° 48.47′; (lanes 9–13) N71° 11.93′ E27° 59.29′, and one individual (lane 14) from Øresund, Denmark. NEAC and NCC are distinguished by their PanI genotype, BB and AA respectively as indicated, while AB can either be NEAC or NCC. For comparison, the related freshwater cod Lota lota (lane 18) that does not have AFGP shows no hybridization.
Figure 1 Southern blot analysis of Atlantic cod genomic DNA showing presence of AFGP coding sequences.TaqI digested genomic DNA (~10–15 μg) from Atlantic cod (lanes 1–14) and polar cod (lanes 15–17) hybridized strongly to a polar cod B. saida AFGP coding sequence probe. Atlantic cod individuals include Norwegian coastal cod (NCC) and North East Arctic cod (NEAC) from the Finnmark coast and marginal Barents Sea sites: (lanes 1–3) N69° 26.91′ E19° 37.56′; (lanes 4–5) N69° 58.34′ E30° 2.37′; (lanes 6–8) N70° 7.24′ E30° 48.47′; (lanes 9–13) N71° 11.93′ E27° 59.29′, and one individual (lane 14) from Øresund, Denmark. NEAC and NCC are distinguished by their PanI genotype, BB and AA respectively as indicated, while AB can either be NEAC or NCC. For comparison, the related freshwater cod Lota lota (lane 18) that does not have AFGP shows no hybridization.CC BY · PubMed Central
Figure 2 Alignment of AFGP-containing scaffolds in Atlantic cod and partial AFGP genomic locus from polar cod. (A) Schematic alignment map—Grey shaded areas indicate regions of high nucleotide identities between polar cod and Atlantic cod. AFGP partial locus of Atlantic cod is represented by two sequence scaffolds (ATLCOD1As00125 and ATLCOD1As03479) in the Newbler assembly (ATLCOD1A), and one sequence scaffold (ATLCOD1Bs1552075) in the Celera assembly (ATLCOD1B). AFGP genes of polar cod and fragmented coding sequences in the cod scaffolds are depicted as red arrows pointing towards the 3′ end. Hypothetical protein-coding genes MAK16-like and RAB14-like are denoted as purple and green arrows, respectively. (B, C) Nucleotide alignments determined using VISTA—The two Atlantic cod sequence scaffolds ATLCOD1As00125 (B) and ATLCOD1As03479 (C) are depicted as connected brown and orange rectangular bars (assembled sequence fragments) and double black bars (gaps between the sequence fragments), generated with UCSC Genome browser. The framed histogram below the Atlantic cod sequence scaffold structures was VISTA generated plots of their alignment with the polar cod partial AFGP locus sequence. Purple areas in the histogram denote conserved AFGP sequences, and grey arrows denote the AFGP genes we annotated in the two Atlantic cod scaffolds. Pink areas denote other conserved regions. In (B) the full length of ATLCOD1As00125 (134,272 bp) was shown. In (C), the first 85 kbp of ATLCOD1As03479 (254,310 bp, reverse complement sequence) was shown; the remaining region of the scaffold did not align with polar AFGP genomic region and therefore not shown. The conserved sequence blocks between Atlantic cod and polar shared very high sequence identities ranging from 80% to 99%, indicative of shared microsynteny.
Figure 2 Alignment of AFGP-containing scaffolds in Atlantic cod and partial AFGP genomic locus from polar cod. (A) Schematic alignment map—Grey shaded areas indicate regions of high nucleotide identities between polar cod and Atlantic cod. AFGP partial locus of Atlantic cod is represented by two sequence scaffolds (ATLCOD1As00125 and ATLCOD1As03479) in the Newbler assembly (ATLCOD1A), and one sequence scaffold (ATLCOD1Bs1552075) in the Celera assembly (ATLCOD1B). AFGP genes of polar cod and fragmented coding sequences in the cod scaffolds are depicted as red arrows pointing towards the 3′ end. Hypothetical protein-coding genes MAK16-like and RAB14-like are denoted as purple and green arrows, respectively. (B, C) Nucleotide alignments determined using VISTA—The two Atlantic cod sequence scaffolds ATLCOD1As00125 (B) and ATLCOD1As03479 (C) are depicted as connected brown and orange rectangular bars (assembled sequence fragments) and double black bars (gaps between the sequence fragments), generated with UCSC Genome browser. The framed histogram below the Atlantic cod sequence scaffold structures was VISTA generated plots of their alignment with the polar cod partial AFGP locus sequence. Purple areas in the histogram denote conserved AFGP sequences, and grey arrows denote the AFGP genes we annotated in the two Atlantic cod scaffolds. Pink areas denote other conserved regions. In (B) the full length of ATLCOD1As00125 (134,272 bp) was shown. In (C), the first 85 kbp of ATLCOD1As03479 (254,310 bp, reverse complement sequence) was shown; the remaining region of the scaffold did not align with polar AFGP genomic region and therefore not shown. The conserved sequence blocks between Atlantic cod and polar shared very high sequence identities ranging from 80% to 99%, indicative of shared microsynteny.CC BY · PubMed Central

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Metadata

Authors
Zhuang, X., Yang, C., Fevolden, S.-E., & Cheng, C.-H. C.
Venue
BMC Genomics
Published
2012-07-02
Volume
13
Issue
1
ISSN
1471-2164
Cited by
12
References
0
Language
en

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CoChat. (2026). Citation check: Protein genes in repetitive sequence—antifreeze glycoproteins in Atlantic cod genome. https://app.cochat.ai/papers/10.1186/1471-2164-13-293
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Zhuang, X., Yang, C., Fevolden, S.-E., & Cheng, C.-H. C. (2012). Protein genes in repetitive sequence—antifreeze glycoproteins in Atlantic cod genome. BMC Genomics. https://doi.org/10.1186/1471-2164-13-293