Evidence map›Paper›PMID 24196410›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2013

Copy number variations of MICAL-L2 shaping gene expression contribute to different phenotypes of cattle.

Yao Xu, Liangzhi Zhang, Tao Shi, Yang Zhou, Hanfang Cai, Xianyong Lan, Chunlei Zhang, Chuzhao Lei, Hong Chen

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Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Copy Number Variation of theAnimals : an open access journal from MDPI · 2022
    Article
  4. Copy Number Variations in theAnimals : an open access journal from MDPI · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. CNV analysis of Meishan pig by next-generation sequencing and effects ofJournal of animal science and biotechnology · 2020
    Article
  9. Article
  10. Associations ofArchives animal breeding · 2019
    Article
  11. Copy number variation (CNV) in theArchives animal breeding · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yao XuShaanxi Key Laboratory of Molecular Biology for Agriculture, College of Animal Science and Technology, Northwest A&F University, No. 22 Xinong Road, Yangling, Xianyang, 712100, Shaanxi, China, xuyao307@gmail.com.
Liangzhi Zhang
Tao Shi
Yang Zhou
Hanfang Cai
Xianyong Lan
Chunlei Zhang
Chuzhao Lei
Hong Chen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Copy number variations (CNVs) recently have been recognized as an important source of genetic variability. Compelling evidence has indicated that CNVs are responsible for phenotypic traits by altering the copy numbers of functional genes. The molecule interacting with CasL-like protein 2 (MICAL-L2) gene plays a critical role in muscle fiber development and has been identified in the CNV region by comparative genomic hybridization array. In the present study, we detected the different distributions of MICAL-L2 gene copy numbers in four Chinese cattle breeds (QC, NY, LX, and CY) and investigated the functional effects of MICAL-L2 CNVs on the gene's expression level and the phenotypic traits in QC and NY cattle. The results showed that the copy number loss (relative to Angus cattle) was more frequent in CY than in the other breeds. The MICAL-L2 gene copy number presented a moderate negative correlation with the transcriptional expression in fetal skeletal muscles (P < 0.05). Statistical analysis revealed that the MICAL-L2 CNVs were significantly associated with body weight, body height, and body length of NY cattle in the early stages (6 and 12 months old), and the copy number loss showed better traits than the gain and/or median groups (P < 0.05). No significance was found at the late stages in QC (24 months old) and NY cattle (18 and 24 months old). These observations provided further insight into the associations between cattle CNVs and economic traits, suggesting that the CNVs may be considered promising markers for the molecular breeding of Chinese beef cattle.

Indexed as

DNA Copy Number VariationsAnimalsBody WeightBreedingCattleFemaleMaleMicrofilament ProteinsMuscle, SkeletalPhenotypeMicrofilament Proteins

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.