FACTORS PREDISPOSING TO ADJACENT 2 AND 3 - 1 DISJUNCTIONS - STUDY OF 161 HUMAN RECIPROCAL TRANSLOCATIONS

被引:57
作者
JALBERT, P
SELE, B
机构
关键词
D O I
10.1136/jmg.16.6.467
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reciprocal translocations produce imbalances by three types of disjunction which are, in decreasing frequency, adjacent 1, 3:1, and adjacent 2. Adjacent 1 disjunction produces duplication deficiencies of inverse topography to those of adjacent 2. The imbalanced chromosome segments in one of these types are balanced in the other. The disjunction 3:1 produces pure trisomies and monosomies. The following situations predispose to adjacent 2 disjunction: translocations between the long arms of two acrocentric chromosomes or between one of these and that of a No 9 chromosome; centric segments, either short or carrying a heterochromatic zone (9qh); a balanced translocation in the mother. The factors predisposing to the disjunction adjacent 2 operate by selection, or directly on the meiotic configuration. Some of them (shortness of the interstitial segment, shortness of the short arms of translocation chromosomes) act in both these ways. Their influence is probably responsible for the repetitive and exclusive character of this disjunction. The conditions for the occurrence of the 3:1 disjunctions seem less strict than those for adjacent 2, although they should be of the same nature (involvement of acrocentrics or a chromosome 9 in the translocation, maternal origin).
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页码:467 / 478
页数:12
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共 151 条
[61]  
HULTEN M, 1974, HEREDITAS, V76, P55
[62]  
HUSTINX TWJ, 1975, ANN GENET-PARIS, V18, P13
[63]  
HUSTINX TWJ, 1974, CLIN GENET, V6, P408
[64]   MULTIPLE CONGENITAL-DEFECTS ASSOCIATED WITH TRISOMY FOR LONG ARM OF NO 4 [J].
ISSA, M ;
POTTER, AM ;
BLANK, CE .
JOURNAL OF MEDICAL GENETICS, 1976, 13 (04) :326-329
[65]   RECIPROCAL TRANSLOCATION, 4Q-/21P+, GIVING RISE TO DOWNS-SYNDROME [J].
JENKINS, MB ;
BOYD, L .
JOURNAL OF MEDICAL GENETICS, 1976, 13 (04) :323-326
[66]   PARTIAL TRISOMY 10P AND FAMILIAL TRANSLOCATION T(7-10)(P22-P12) [J].
JOHNSON, G ;
BACHMAN, R ;
ROED, T ;
RIDDERVOLD, P .
HUMAN GENETICS, 1977, 35 (03) :353-356
[67]  
JOHNSON G, 1976, HUM GENET, V34, P103
[68]   NEW CASE OF TRISOMY FOR DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9-13)(P21-Q21) [J].
JOTTERAND, M ;
JUILLARD, E .
HUMAN GENETICS, 1976, 33 (03) :213-222
[69]   CHROMOSOME ANOMALIES IN 3 SUCCESSIVE ABORTUSES DUE TO PATERNAL TRANSLOCATION, T(13Q-18Q+) [J].
KAJII, T ;
MEYLAN, J ;
MIKAMO, K .
CYTOGENETICS AND CELL GENETICS, 1974, 13 (05) :426-436
[70]   47,XY,+DER(11-22)(Q23-Q12) FOLLOWING BALANCED TRANSLOCATION T(11-22)(Q23-Q12) MAT - REMARKS ON PROBLEM OF TRISOMY-22 [J].
KESSEL, E ;
PFEIFFER, RA .
HUMAN GENETICS, 1977, 37 (01) :111-116