Zebrafish as a Model for Osteoporosis: Functional Validations of Genome-Wide Association Studies

被引:4
|
作者
Ben-Zvi, Inbar [1 ]
Karasik, David [1 ]
Ackert-Bicknell, Cheryl L. [2 ]
机构
[1] Bar Ilan Univ, Azrieli Fac Med, Musculoskeletal Genet Lab, Safed, Israel
[2] Univ Colorado, Dept Orthoped, Aurora, CO USA
关键词
Zebrafish (Danio rerio); Genome-wide association study (GWAS); Bone mineral density (BMD); Osteoporosis; Synteny; BONE-MINERAL DENSITY; LOCI; METAANALYSIS; OSTEOGENESIS; EXPRESSION; EVOLUTION; SEQUENCE; INSIGHTS; VARIANTS; REVEAL;
D O I
10.1007/s11914-023-00831-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of Review GWAS, as a largely correlational analysis, requires in vitro or in vivo validation. Zebrafish (Danio rerio) have many advantages for studying the genetics of human diseases. Since gene editing in zebrafish has been highly valuable for studying embryonic skeletal developmental processes that are prenatally or perinatally lethal in mammalian models, we are reviewing pros and cons of this model.Recent Findings The true power for the use of zebrafish is the ease by which the genome can be edited, especially using the CRISPR/Cas9 system. Gene editing, followed by phenotyping, for complex traits such as BMD, is beneficial, but the major physiological differences between the fish and mammals must be considered. Like mammals, zebrafish do have main bone cells; thus, both in vivo stem cell analyses and in vivo imaging are doable. Yet, the "long" bones of fish are peculiar, and their bone cavities do not contain bone marrow. Partial duplication of the zebrafish genome should be taken into account.Summary Overall, small fish toolkit can provide unmatched opportunities for genetic modifications and morphological investigation as a follow-up to human-first discovery.
引用
收藏
页码:650 / 659
页数:10
相关论文
共 50 条
  • [1] Zebrafish as a Model for Osteoporosis: Functional Validations of Genome-Wide Association Studies
    Inbar Ben-Zvi
    David Karasik
    Cheryl L. Ackert-Bicknell
    Current Osteoporosis Reports, 2023, 21 : 650 - 659
  • [2] Mouse Models and Online Resources for Functional Analysis of Osteoporosis Genome-Wide Association Studies
    Maynard, Robert D.
    Ackert-Bicknell, Cheryl L.
    FRONTIERS IN ENDOCRINOLOGY, 2019, 10
  • [3] Future of Osteoporosis Genetics: Enhancing Genome-Wide Association Studies
    Farber, Charles R.
    Lusis, Aldons J.
    JOURNAL OF BONE AND MINERAL RESEARCH, 2009, 24 (12) : 1937 - 1942
  • [4] A dynamic model for genome-wide association studies
    Kiranmoy Das
    Jiahan Li
    Zhong Wang
    Chunfa Tong
    Guifang Fu
    Yao Li
    Meng Xu
    Kwangmi Ahn
    David Mauger
    Runze Li
    Rongling Wu
    Human Genetics, 2011, 129 : 629 - 639
  • [5] A dynamic model for genome-wide association studies
    Das, Kiranmoy
    Li, Jiahan
    Wang, Zhong
    Tong, Chunfa
    Fu, Guifang
    Li, Yao
    Xu, Meng
    Ahn, Kwangmi
    Mauger, David
    Li, Runze
    Wu, Rongling
    HUMAN GENETICS, 2011, 129 (06) : 629 - 639
  • [6] Integrative functional linear model for genome-wide association studies with multiple traits
    Li, Yang
    Wang, Fan
    Wu, Mengyun
    Ma, Shuangge
    BIOSTATISTICS, 2022, 23 (02) : 574 - 590
  • [7] Insights into the genetics of osteoporosis from recent genome-wide association studies
    Zheng, Hou-Feng
    Spector, Timothy D.
    Richards, J. Brent
    EXPERT REVIEWS IN MOLECULAR MEDICINE, 2011, 13
  • [8] Genetics of osteoporosis from genome-wide association studies: advances and challenges
    J. Brent Richards
    Hou-Feng Zheng
    Tim D. Spector
    Nature Reviews Genetics, 2012, 13 : 576 - 588
  • [9] Genome-wide association studies
    Nature Reviews Methods Primers, 1
  • [10] Genome-wide association studies
    Willson, Joseph
    NATURE REVIEWS METHODS PRIMERS, 2021, 1 (01):