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Patterns of expression of the X -chromosome photopigment genes and implications for normal and defective color vision.

机译:X染色体光色素基因的表达模式及其对正常和有缺陷的色觉的影响。

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摘要

Deutan color vision defects are caused by the lack of a contribution from one of the three spectrally sensitive classes of cone photoreceptor. People who are deutan color blind lack middle wavelength (M) cone function and retain function of the long wavelength sensitive (L) and short wavelength sensitive (S) cone photoreceptors. The L and the M photopigment genes are highly homologous and occur in a tandem array on the X-chromosome. These genes have therefore been subject to numerous unequal recombination events that have led to gene duplications and deletions. A known cause of deutan color blindness is the loss of the M photopigment genes. However, most people who are deutan have genes the encode the M photopigment. For these people the cause of color blindness has remained unknown. Through the work in this thesis, a deleterious mutation was found within the M photopigment genes of two deutan subjects that accounts for the lack of M cone function in these individuals. In addition, in cases where a deleterious mutation was not apparent, individuals were found to have a gene array that contained two L genes and the M gene was positioned last. Position of an L or M gene last within a gene array that contained three genes was correlated with an absence of expression derived from that gene. These experiments led to appreciation for the importance of the structure of the photopigment gene array itself in determining the expression pattern of the L and M genes. The hypothesis that cis-acting factors within the gene array control variation in L versus M photopigment gene expression across the population was then tested within the female retina. Strong evidence was found in favor of factors that occur within the photopigment gene array determining the ratio of expression of the L and M genes. Through the analysis of photopigment gene expression in the female retina, the size of the X-chromosome inactivation patches was estimated for the cone photoreceptor mosaic.
机译:Deutan彩色视觉缺陷是由于缺少三种对光谱敏感的视锥光感受器之一造成的。 Deutan色盲患者缺乏中波长(M)视锥细胞的功能,而保留了长波长敏感(L)和短波敏感(S)视锥细胞的功能。 L和M光色素基因高度同源,并以串联排列的形式出现在X染色体上。因此,这些基因经历了许多不平等的重组事件,这些事件导致了基因的重复和缺失。 Deutan色盲的一个已知原因是M光色素基因的丢失。但是,大多数为犹太人的人都有编码M色素的基因。对于这些人来说,色盲的原因仍然未知。通过本论文的工作,在两个德国人的M色素基因中发现了一个有害的突变,这说明这些个体缺乏M视锥细胞功能。另外,在有害突变不明显的情况下,发现个体具有包含两个L基因的基因阵列,并且M基因位于最后。包含三个基因的基因阵列中最后一个L或M基因的位置与该基因的表达缺失相关。这些实验导致人们认识到光色素基因阵列本身的结构在确定L和M基因表达模式中的重要性。然后在雌性视网膜内测试了基因阵列内的顺式作用因子控制整个群体中L对M光色素基因表达变化的假说。发现有强有力的证据支持光色素基因阵列内存在的因素决定了L和M基因的表达比例。通过分析雌性视网膜中的光色素基因表达,估计了锥体感光体镶嵌的X染色体失活斑块的大小。

著录项

  • 作者单位

    The Medical College of Wisconsin.;

  • 授予单位 The Medical College of Wisconsin.;
  • 学科 Molecular biology.;Neurosciences.
  • 学位 Ph.D.
  • 年度 2001
  • 页码 163 p.
  • 总页数 163
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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